(Q33593904)

English

Sex reversal in a child with a 46,X,Yp+ karyotype: support for the existence of a gene(s), located in distal Xp, involved in testis formation

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Sex reversal in a child with a 46,X,Yp+ karyotype: support for the existence of a gene(s), located in distal Xp, involved in testis formation (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

0 references

author name string

Ogata T

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Hawkins JR

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Taylor A

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Matsuo N

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Hata J

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Goodfellow PN

6

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

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publication date

1 April 1992

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

29

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

226-230

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Female phenotype and multiple abnormalities in sibs with a Y chromosome and partial X chromosome duplication: H--Y antigen and Xg blood group findings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Inherited partial X chromosome duplication in a mentally retarded male

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Male sexual differentiation in mice lacking H-Y antigen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Characterization of the human factor VIII gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Structure and Expression of a Complementary DNA for the Nuclear Coded Precursor of Human Mitochondrial Ornithine Transcarbamylase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Isolation of a sequence which maps close to the human sex determining gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Inherited X-chromosome inverted tandem duplication in a male traced to a grandparental mitotic error

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

A new syndrome with mental retardation, short stature and an Xq duplication.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

An RFLP detecting single copy X-chromosome fragment, dic56, from Xp22-Xpter [HGM8 assignment no. DXS 143].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

The pseudoautosomal boundary in man is defined by an Alu repeat sequence inserted on the Y chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Comparison of human ZFY and ZFX transcripts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

A human XY female with a frame shift mutation in the candidate testis-determining gene SRY.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Genetic evidence equating SRY and the testis-determining factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Duplications of the X chromosome in males: evidence that most parts of the X chromosome can be active in two copies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Localization of the X inactivation centre on the human X chromosome in Xq13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Systemic lupus erythematosus associated with klinefelter's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

DNA sequencing with chain-terminating inhibitors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

21 June 2018

Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015917

30 October 2018

Improvement of trypsin method for banding chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Facing up to the Chernobyl accident

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Separation of the genetic loci for the H–Y antigen and for testis determination on human Y chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A pseudoautosomal gene in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypervariable telomeric sequences from the human sex chromosomes are pseudoautosomal

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-ring Turner's syndrome with combined immunodeficiency and selective gonadotropin defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a panel of highly variable minisatellites cloned from human DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Systemic lupus erythematosus in a woman with primary 47XXX hypogonadism]

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited tandem duplication dup(X) (q131-q212) in a male proband

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inhibitory effect of ethidium bromide on mitotic chromosome condensation and its application to high-resolution chromosome banding

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tandem duplication dup(X)(q13q22) in a male proband inherited from the mother showing mosaicism of X-inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rapid banding technique for human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1583640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.29.4.226

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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