(Q33668658)

28 July 2017

1 reference

title

Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome (English)

1 reference

28 July 2017

Davis RM

1

1 reference

PubMed ID

7017147

28 July 2017

language of work or name

English

0 references

publication date

1 June 1981

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

18

1 reference

28 July 2017

161-195

1 reference

28 July 2017

3

1 reference

TRIPLOID INTERSEXES IN DROSOPHILA MELANOGASTER

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Genetic Analysis of the Male Fertility Factors on the Y Chromosome of Drosophila Melanogaster

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

THE Y-CHROMOSOME AS THE BEARER OF MALE DETERMINING FACTORS IN THE MOUSE

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

EXCEPTIONAL INHERITANCE OF A SEX-LINKED GENE IN THE MOUSE EXPLAINED ON THE BASIS THAT THE X/O SEX-CHROMOSOME CONSTITUTION IS FEMALE

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

21 June 2018

An XXY male in the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A child with 49 chromosomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A case of human intersexuality having a possible XXY sex-determining mechanism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Two conceptions in a 45,X woman

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A New Variant of Klinefelter's Syndrome with a Presumptive Deleted Y Chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Presumptive Y/D translocation in mixed gonadal dysgenesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Racial differences in the length of the human Y chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Chromosome mosaicism in a hermaphrodite

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

8 cases of XO-XY mosaicism, one XO-XYq--with gonadoblastoma

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Isochromosome for long arm of Y chromosome in patient with Turner's syndrome and sex chromosome mosaicism (45,X-46,XYqi)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A case of dicentric Y in a male pseudohermaphrodite with complex gonosomal mosaicism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

XO-XY-Xy mosaicism and Turner's syndrome in an 18-year-old girl

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A patient with 45,X-46,XXq--46,XXq-dic karyotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Normal male development with Y chromosome long arm deletion (Yq-)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XYqdic, in a patient with features of Turner's syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Structural abnormalities and role of the Y chromosome in man

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Structural abnormalities of the sex chromosomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

21 June 2018

Mosaics and chimaeras

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Population cytogenetic investigation of newborns in Moscow.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Male pseudohermaphroditism with 45X-46XYq- mosaicism in a pair of monozygotic twins.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Deletion of the long arms of the Y chromosome with normal male development and intelligence

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Apparent pseudopuberty in a phenotypic female with a gonadal tumor and an autosome-Y chromosome translocation.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Probable origin of a satellited Y chromosome found in a French-Canadian family

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Renovascular hypertension. Prospective diagnostic yield in a random access population.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A familial Y-22 translocation in man.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A "Philadelphia-like" chromosome derived from the Y in a patient with refractory dysplastic anemia.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Human dicentric Y chromosomes. Case report and review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Localization of male determining factor on short arm of Y chromosome Case report of a baby with 46, x, t (Yp+;14q-)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A human satellited Y chromosome with a probably illegitimate paternal origin.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Analytic review: nature and origin of males with XX sex chromosomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Abnormalities of human sex chromosomes. I. A ring Y without mosaiciam

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

13q+ chromosome due to a probable translocation of a supernumerary Y

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Hereditary transmission for 300 years of a satellited Y chromosome in a family

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Research on the origin of a small Y chromosome several hundred years old

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Eosinophilic Leukemia with Fibrosing Endocarditis and Short Y Chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Turner's syndrome and 46,X,i(Yq) karyotype.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Prenatal evaluation in a case of familial Y chromosome long arm deletion (Yq-).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A Y-autosome translocation 46,X,t(Yq-7q+) associated with multiple congenital anomalies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Occurrence of tumors in dysgenetic gonads

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Gonadoblastoma. A review of 74 cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Chromosome studies on testicular cells from 50 subfertile men.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaics.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Robertsonian translocation between the chromosome Y and 15.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Lateral asymmetry in the fluorescence of human Y chromosomes stained with 33 258 Hoechst

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Presumptive Y-15 translocation and mental retardation in a family with a case of Klinefelter's syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

An eleven-generation satellited Y chromosome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Quinacrine fluorescence of the human Y chromosome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Chromosome measurements on an XXp+ male

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

The age of occurrence of gonadal tumors in intersex patients with a Y chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A (Y;15) translocation, 46 chromosomes. Repository identification No. GM-118

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Mosaicism and lack of fluorescence of Y chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Possible role for H--Y antigen in the primary determination of sex

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Dicentric Yp chromosome in a patient with the gonadal dysgenesis and gonadoblastoma

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Gonadal dysgenesis and abnormalities of the human sex chromosomes: current status of phenotypic-karyotypic correlations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Translocation 46,X, t(Y;7)(q122;q11) in a case of male sterility

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Increased frequency of heterozygotes for α1 antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

45,X/ 46,XX/ 46,XY Mosaic with female phenotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Serologic detection of a y-linked gene in xx males and xx true hermaphrodites

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Ring Y chromosome: 45,X/46,Xr(Y) chromosome mosaicism in a phenotypically normal male with azoospermia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Translocation of the Y chromosome to an autosome in a boy with hypogonadism (author's transl)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A man with presumptive Y/Y translocation, observed in a forensic psychiatric department.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Ring Y chromosome without mosaicism.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A mitotically unstable human dicentric Y chromosome in a male pseudohermaphrodite

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Chromosome studies in couples with repeated spontaneous abortions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Contraceptives and the conceptus. I. Chromosome abnormalities of the fetus and neonate related to maternal contraceptive history

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Mapping the locus of the H-Y gene on the human Y chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

X/XYq - mosaicism and mixed gonadal dysgenesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Yq deletion, aspermia, and short stature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Nonmosaic 46,X,r(Y) karyotype with female phenotype.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Male with 45,X karyotype.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Meiotic chromosomes in an infertile male with an unbalanced Y/13 translocation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Gonadal dysgenesis with 45,X/46,X,dic(Yp) mosaicism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Testis-determining H-Y antigen in XO males of the mole-vole (Ellobius lutescens)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Y to X translocation in man

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Four new cases of Dicentric Y chromosomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Evidence for an association between univalent Y chromosomes and spermatoycte loss in XYY mice and men.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Cytogenetic polymorphism or Y/15 translocation in a black male with ambiguous genitalia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A case of a reciprocal translocation between the Y and no. 1 chromosomes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Length heteromorphisms of fluorescent (f) and non-fluorescent (nf) segments of human Y chromosome: classification, frequencies, and incidence in normal Caucasians

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Inconsistent expression of both centromeres of a dicentric Y chromosome in a child with ambiguous external genitalia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

BSu restriction of DNA from cases exhibiting sex-chromosome abnormalities

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Y autosome translocation and complex chromosome rearrangement in cri du chat syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

XO/XY mosaicism with non fluorescent Y chromosome: clinical, cytogenetic and endocrinological studies on a female subject

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Nullisomy for the distal portion of Xp in a male child with a X/Y translocation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Mosaicism presumably related to a Y/6 translocation in a boy with multiple congenital abnormalities

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Human male infertility, probably genetically determined, due to defective meiosis and spermatogenic arrest

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Sexual and somatic determinants of the human Y chromosome: studies in a 46,XYp- phenotypic female

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A (Y;17) translocation in a fibroblast culture from a female with 46 chromosomes. Repository identification No. GM-2598

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Prenatal diagnosis of a de novo Y/22 translocation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Unstable dicentric iso(Yq) chromosome in a pseudohermaphrodite

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

The 48,XXXX/49,XXXXY/49,XXXX,i(Yq) mosaicism in a 3-year-old boy from a twin pregnancy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Structural abnormalities of the Y chromosome. Observations in ten cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Sixteen years' experience of counselling, diagnosis, and prenatal detection in one genetic centre: progress, results, and problems

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Assignment of the H-Y antigen gene to the short arm of chromosome Y

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Confirmation of Y/autosome translocations using recombinant DNA

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Deletion of the long arm of the Y chromosome and multiple malformations. Description of a case

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

The role of the H-Y antigen in human sexual development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Translocation of a supernumerary Y to a 15: Study of six cases (three males and three females) in three generations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Unstable ring Y chromosome in an aspermic male

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Chromosome survey of newborn infants in Tokyo: follow-up study for XYY

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A 45 X/46 X dic (Yq) puberal male without genital ambiguity. Critical study of the peculiarities of his phenotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Three cases of sex chromosome mosaicism with a nonfluorescent Y

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

An azoospermic male with a Y/Autosome translocation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

H-Y antigen and the genetics of sex determination

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Satellited Y chromosome (Yqs) and nucleolar organizer occurring de novo

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A satellited Y chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A theory explaining the abnormality in 45,X/46,XY mosaicism with non-fluorescent Y chromosome. presentation of three cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

45,X/46,X,dic(Yq) mosaicism and mixed gonadal dysgenesis. Case report and review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Dicentric Y chromosome in a male pseudohermaphrodite 45,X/46,X, dic (Y)/47, XYY

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Appearance of hCG-receptor after conversion of newborn ovarian cells into testicular structures by H-Y antigen in vitro

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Comparative studies in two cases of testicular feminization syndrome, one with and the other without the fluorescent distal band q12 of the Y

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Silver stain reveals nucleolus organizer regions on a satellited Yq chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A satellited Yq chromosome associated with trisomy 21 and an inversion of chromosome 9

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Mosaic form of deletion of the long arm of Y chromosome in Down's syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

H-Y gene expression in apparent absence of the long arm of the Y chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Reassessment of presumed Y/22 and Y/15 translocations in man using a new technique

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Testicular cells lysostripped of H-Y antigen organize ovarian follicle-like aggregates

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Localisation of a male-specific DNA fragment to a sub-region of the human Y chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Cytogenetics and somatic cell genetics: the impact of chromosome banding

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

N-Band polymorphism of human acrocentric chromosomes and its relevance to satellite association

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Non-fluorescent Y chromosome in a male infant with Turner's symptoms and XO/XY mosaicism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

C and Q bands in long arm of Y chromosomes; are they identical?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Oligozoospermia: a seven-year survey of the incidence, chromosomal aberrations, treatment and pregnancy rate

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Deletion of Y Chromosome in a Family with Muscular Dystrophy and Hypospadias

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

A SEX CHROMATIN NEGATIVE INDIVIDUAL WITH CHROMOSOMES (XO) PLUS A PERSISTENT CENTRIC FRAGMENT.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

XO-XY CHROMOSOME MOSAICISM.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Structural exchange between the X and Y chromosomes as the probable cause of hypogonadism

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Length of the Y chromosome in a general male population

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Y ring chromosome associated with gonadoblastoma in situ

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

De novo translocation t(Yq-; 15p+) in a malformed boy

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Unusual in vivo rearrangements of the Y chromosome with mitotic instability in vitro

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048703

Structural abnormalities of the Y chromosome and abnormal external genitals

30 October 2018

1 reference

12 December 2020

Letter: Possible evidence for Xp plus in and XX Male

1 reference

12 December 2020

Pericentric Y inversion in the general population

1 reference

12 December 2020

Possible evidence of X-Y interchange in an XX male

1 reference

12 December 2020

Structural variation in human nitotic chromosomes

1 reference

12 December 2020

Pitfalls in prenatal diagnosis resulting from chromosomal mosaicism

1 reference

12 December 2020

45, XO/46, XYq dic mosaicism in a patient with ambiguous genitalia

1 reference

12 December 2020

Familial translocation 22/Y and partial autosomal trisomy in a young girl

1 reference

12 December 2020

A probable partial deletion of the Y chromosome in an intersex patient

1 reference

12 December 2020

The spectrum of gonadal dysgenesis. A clinical, cytogenetic, and pathologic study

1 reference

12 December 2020

X-XY mosaicism with short y

1 reference

12 December 2020

Organization in vitro of ovarian cells into testicular structures

1 reference

12 December 2020

[Male pseudohermaphroditism and mosaicism 45,X-46,XYdic-46,XXq-]

1 reference

12 December 2020

[Genetics of sex differentiation in humans]

1 reference

12 December 2020

Non-fluorescence of the Y-chromosome

1 reference

12 December 2020

A phenotypic male with karyotype 45,X/45,X,ace+(?Yq-)

1 reference

12 December 2020

Abnormal sexual development associated with sex chromosome mosaicism. Report of three cases

1 reference

12 December 2020

Probable long-arm deletion of Y chromosome in boy of short stature

1 reference

12 December 2020

XO and male phenotype

1 reference

12 December 2020

Subdivision of the human Y chromosome

1 reference

12 December 2020

X-autosome translocation with a 47,XXXY qs,t(9p-;Xq+) karyotype

1 reference

12 December 2020

KARYOTYPES OF 130 CHILDLESS MEN

1 reference

12 December 2020

Non-fluorescent Y chromosome in a 45,X-46,XY mosaic

1 reference

12 December 2020

Heteromorphic X Chromosomes in 46,XX males?

1 reference

12 December 2020

Cytogenetic and clinical notes on a girl with a 46,X,i(Yq) karyotype, H-Y antigen-negative, and a gonadoblastoma

1 reference

12 December 2020

Triple mosaicism with an isochromosome derived from a partially deleted Y in a male pseudohermaphrodite

1 reference

12 December 2020

Sex chromosome anomalies detection and fluorescence

1 reference

12 December 2020

Mitotic and meiotic analysis of an Y-autosome translocation(author's transl)

1 reference

12 December 2020

Length variation in the quinacrine-binding segment of human Y chromosomes of different sizes

1 reference

12 December 2020

Monolateral gonadal dysgenesis with X00-XY mosaicism

1 reference

12 December 2020

Isochromosome for the long arm of the Y in an infertile male

1 reference

12 December 2020

Non-fluorescent and non-heterochromatic Y chromosome in 45, X 46,XY mosaicism

1 reference

12 December 2020

Quinacrine fluorescence of variant and abnormal human Y chromosomes

1 reference

12 December 2020

Mitotic behavior of a human dicentric Y chromosome

1 reference

12 December 2020

Y chromosome fluorescence in phenotypic females

1 reference

12 December 2020

Streak gonads and the Y chromosome

1 reference

12 December 2020

Heteromorphic X chromosomes in 46,XX males: Evidence for the involvement of X-Y interchange

1 reference

12 December 2020

Problems in prenatal diagnosis resulting from chromosomal mosaicism

1 reference

12 December 2020

Y to X translocation in a woman with reproductive failure. A new rearrangement

1 reference

12 December 2020

Studies on the function of H-Y antigen: dissociation and reorganization experiments on rat gonadal tissue

1 reference

12 December 2020

A rare structural anomaly of the Y chromosome: Y ring (author's transl)

1 reference

12 December 2020

CLINICAL AND CYTOGENETICAL STUDIES IN FEMALE GONADAL DYSGENESIS AND THEIR BEARING ON THE CAUSE OF TURNER'S SYNDROME

1 reference

12 December 2020

Abnormal Y chromosomes and monosomy 45,X: a concept derived from the study of three patients

1 reference

12 December 2020

XO/XY mosaicism and non-fluorescing Y chromosome in a male

1 reference

12 December 2020

45,X-46,Xr(Y) in a case of asymmetrical testicular differentiation

1 reference

12 December 2020

Y-21 translocation with gonadal and renal dysgenesis and cardiac rupture

1 reference

12 December 2020

Short Y chromosome and Ph1 chromosome in acute monomyelocytic leukaemia

1 reference

12 December 2020

True hermaphroditism: a clinical description and a proposed function for the long arm of the Y chromosome

1 reference

12 December 2020

Structural aberrations of the X chromosome in man

1 reference

12 December 2020

Y/22 translocation in a YY male

1 reference

12 December 2020

[Transmission of a small Y through 11 generations in a familial line]

1 reference

12 December 2020

A patient with a dicentric Y chromosome

1 reference

12 December 2020

Cytological Evidence for the Association of the Short Arms of the X and Y Chromosomes in the Human Male

1 reference

12 December 2020

H-Y antigen-positive male pseudohermaphroditism with 45,X/46,XYq-mosaicism

1 reference

12 December 2020

Father and son with karyotype 47,XY,?Yq-

1 reference

12 December 2020

Y/autosomal translocations

1 reference

12 December 2020

Quinacrine mustard fluorescence of a second Y chromosome in a Y-autosomal translocation

1 reference

12 December 2020

Structural Abnormalities of the Y Chromosome in Man

1 reference

12 December 2020

A satellited human Y chromosome: an evidence of autosome gonosome translocation. A preliminary note

1 reference

12 December 2020

Meiotic studies on a subfertile patient with a ring Y chromosome

1 reference

12 December 2020

Detection of sex-chromosome anomalies in newborn infants (author's transl)

1 reference

12 December 2020

Communications and commentaries: A 46,XYq- male with aspermia

1 reference

12 December 2020

Histopathologic Study with Cytogenetic Correlation in 20 Cases of Gonadal Dysgenesis

1 reference

12 December 2020

Satellites on the long Y chromosome arm: a familial Y-autosome translocation in man

1 reference

12 December 2020

The Y-linked H-Y antigen locus and the X-linked Tfm locus as major regulatory genes of the mammalian sex determining mechanism

1 reference

12 December 2020

Gonadoblastoma occurring in a female with XO/XY fragment gonadal dysgenesis

1 reference

12 December 2020

Sex chromosome mosaicism of X/XY or X/XY/XYY

1 reference

12 December 2020

45,X-45,X, ace(?Yp)plus-46,X,r(Y) in a phenotypically normal newborn male

1 reference

12 December 2020

Antenatal genetic diagnosis in a kindred with a 15p plus chromosome

1 reference

12 December 2020

A boy with 46, X, del, Y, due to a de nove mutation

1 reference

12 December 2020

Cytogenetical and clinical investigations in four subjects with anomalies of sexual development

1 reference

12 December 2020

Cytogenetics and infertility in man. II. Testicular histology and meiosis

1 reference

12 December 2020

[A case of primary amenorrhea with predominant Y-D translocation]

1 reference

12 December 2020

Gonadal dysgenesis associated with a very rare XO-X+ "fragment" chromosomal mosaicism (a case report)

1 reference

12 December 2020

Length of the Y chromosome in criminal males

1 reference

12 December 2020

A case of ring Y chromosome

1 reference

12 December 2020

CHROMOSOME STUDIES ON TESTICULAR TISSUE CULTURES AND BLOOD LEUKOCYTES OF A MALE PREVIOUSLY REPORTED TO HAVE NO Y CHROMOSOME

1 reference

12 December 2020

A strongly fluorescing abnormal chromosome in a malformed child

1 reference

12 December 2020

Centromere inactivation in a case of turner variant with two dicentric iso-long arm Y chromosomes

1 reference

12 December 2020

Essential testicle hypotrophy, confluent sebaceous adenomatosis of the face, caryotype 46,XY-46,XYpi-47,XYpiYpi

1 reference

12 December 2020

Induction of distinctive chromosomal bands in selected human subjects with D, G, and Y chromosome anomalies

1 reference

12 December 2020

Translocation Y/5 resulting in Cri du Chat syndrome

1 reference

12 December 2020

XO-XY mosaicism and nonfluorescent Y chromosome

1 reference

12 December 2020

1 reference

12 December 2020

Hypogonadism Associated with Chromosomal Break in Autosome No. 2 and Translocation Presumably on the Y Chromosome

1 reference

12 December 2020

CLINICAL, HISTOLOGIC, AND CYTOGENETIC FINDINGS IN MALE HERMAPHRODITISM. I. MALE HERMAPHRODITISM WITH AMBIGUOUS OR PREDOMINANTLY MASCULINE EXTERNAL GENITALIA

1 reference

12 December 2020

Isochromosome Y [46, X, i(Yq)] and female phenotype

1 reference

12 December 2020

A boy with 47,X,del(X)(p11leads to q13:q21leads to q24),del(Y)(q11):reexamination of a case previously described as 47,XX,?Yq-

1 reference

12 December 2020

An unusual sex chromatin pattern in three mentally deficient subjects

1 reference

12 December 2020

Polymorphism of the human Y chromosomes: fluorescence microscopic studies on the sites of morphologic variation

1 reference

12 December 2020

45,X/46,SYq dic-Sexchromosome mosaic

1 reference

12 December 2020

Structural aberrations of the Y chromosome and the corresponding phenotype. Report of a case with the karotype 45,X-46,X,i(Yp)

1 reference

12 December 2020

A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities

1 reference

12 December 2020

Gonadoblastoma (gonocytoma 3). Report of a case

1 reference

12 December 2020

Translocation t(Y;14) in an azoospermic man

1 reference

12 December 2020

Triple chromosomal mosaic in a woman with clinical evidence of a masculinisation

1 reference

12 December 2020

[Deviations in the sex chromosome findings of a rare special form of intersexuality with missing internal genital organs]

1 reference

12 December 2020

A Presumptive Y-Autosome Translocation in a Boy With Congenital Malformations

1 reference

12 December 2020

Isochromosome Yq in a woman with atypical Turner's syndrome

1 reference

12 December 2020

Mixed gonadal dysgenesis with Turner phenotype and XO-XYq- mosaicism

1 reference

12 December 2020

The anatomy and histology of XO human embryos and fetuses

1 reference

12 December 2020

Chromosome aberrations in XO-XY mosaic individuals and their fathers

1 reference

12 December 2020

Prepubertal XY gonadal dysgenesis

1 reference

12 December 2020

A male pseudohermaphrodite with a dicentric Y chromosome. Autoradiographic study

1 reference

12 December 2020

Fluorescence pattern of a dicentric Y

1 reference

12 December 2020

H-Y antigen: localization of the H-Y gene

1 reference

12 December 2020

Y-Autosome Translocation, Gonadal Dysgenesis, and Gonadoblastoma

1 reference

12 December 2020

Familial transmission of a translocation Y/14

1 reference

12 December 2020

Letter: Brilliantly fluorescing enlarged short arms D or G

1 reference

12 December 2020

Three dicentric Y chromosomes

1 reference

12 December 2020

Mitotic and meiotic studies on 70 cases of male sterility (author's transl)

1 reference

12 December 2020

[Trisomy 21 and metacentric Y]

1 reference

12 December 2020

[Cheilognatho-urano-staphyloschisis associated with t(Y;13)]

1 reference

12 December 2020

Bilateral gonadoblastoma in a phenotypic female with 45,X/46,X, dicentric iso Y [45,X/46,X,idic(Yq)] mosaicism

1 reference

12 December 2020

Y-chromosomal genes in a phenotypic male with a 46XX karyotype

1 reference

12 December 2020

Non-fluorescent Y-chromosome

1 reference

12 December 2020

Cytogenetics and infertility in man. I. Karyotype and seminal analysis: results of a five-year survey of men attending a subfertility clinic

1 reference

12 December 2020

[Familial mosaicism with G ring]

1 reference

12 December 2020

Gonadal dysgenesis and its unilateral variant with testis in monozygous twins: related to discordance in sex chromosomal status

1 reference

12 December 2020

[Human diseases caused by chromosomal aberrations.]

1 reference

12 December 2020

Familial Y/22 translocation in a woman

1 reference

12 December 2020

CYTOGENETIC STUDIES IN LEUCOCYTES ON THE GENERAL POPULATION: SUBJECTS OF AGES 65 YEARS AND MORE

1 reference

12 December 2020

[Klinefelter's syndrome and hypospadias. Presence of 2 X chromosomes. Rupture of Y chromosome and translocation of its fragments.]

1 reference

12 December 2020

Sex determination and gonadal differentiation in man. A unifying concept of normal and abnormal sex development

1 reference

12 December 2020

A familial Y/autosome translocation in man

1 reference

12 December 2020

Letter: Y-to-X translocation in a girl

1 reference

12 December 2020

X"Y"-XO MOSAICISM IN A PHENOTYPIC INTERSEX; REPORT OF A CASE

1 reference

12 December 2020

Presumptive Y-15 and Y-22 translocation in two families

1 reference

12 December 2020

Constancy of the length of human Y chromosome

1 reference

12 December 2020

Identifiers

0 references

1 reference

28 July 2017

1 reference

PubMed ID

7017147