(Q33585184)

28 July 2017

1 reference

title

KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS (English)

1 reference

28 July 2017

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1 reference

1 reference

Malcolm Ferguson-Smith

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ORCID Public Data File 2021

author name string

FERGUSON-SMITH MA

series ordinal

1

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PubMed ID

14295659

28 July 2017

language of work or name

English

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publication date

1 June 1965

1 reference

Journal of Medical Genetics

28 July 2017

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28 July 2017

2

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28 July 2017

142-155

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28 July 2017

2

1 reference

Evidence that the Xg blood group genes are on the short arm of the X chromosome

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012851

Gene action in the X-chromosome of the mouse (Mus musculus L.)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012851

Chromosomal studies of patients with congenital anomalies simulating those of gonadal aplasia, including a case of true gonadal and sex reversal

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012851

Congenital anomalies associated with gonadal aplasia; review of 55 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=1012851

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=1012851

The occurrence of sex chromatin in early human and macaque embryos

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012851

21 June 2018

The Chromosomes of Man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012851

The triple-X syndrome. Clinical, pathological, and chromosomal studies in three mentally retarded 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=1012851

XO-XY CHROMOSOME MOSAICISM.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012851

Sex-chromosome abnormalities in a population of mentally defective children.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012851

A new variant of human intersex with discussion on the developmental aspects.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012851

[The syndrome of multiple malformations associated with gonadal dysgenesis (Turner syndrome) with XO chromosome formula.]

31 October 2018

1 reference

12 December 2020

Triple mosaicism of the sex chromosomes in Turner's syndrome and Hirschsprung's disease

1 reference

12 December 2020

[Presumption of monozygotism in spite of a sexual dimorphism: XY male subject and haploid X neuter subject.]

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Multiple congenital defects in a twelve year old boy with cryptorchidism--"male Turner's syndrome"

1 reference

12 December 2020

[Male Turnerian pseudohermaphroditism]

1 reference

12 December 2020

[A case of chromatin-negative XY-XX mosaicism with gonadal dysgenesis and female phenotype sex]

1 reference

12 December 2020

[A recent case of XX/XO in a case of Turner's syndrome.]

1 reference

12 December 2020

[Germinal aplasia and dwarfism.]

1 reference

12 December 2020

Syndrome of gonadal dysgenesis and abdominal testis with an XO/XY chromosome mosaicism

1 reference

12 December 2020

Apparent masculinization of the female fetus diagnosed as true hermaphrodism by chromosomal studies

1 reference

12 December 2020

A patient suffering from Turner's syndrome and acromegaly

1 reference

12 December 2020

[A recent case of "non-functioning ovaries".]

1 reference

12 December 2020

GONADAL DYSGENESIS WITH XUXX MOSAICISM AND A POSITIVE SEX CHROMATIN PATTERN

1 reference

12 December 2020

THE PATHOLOGY AND CYTOGENETICS OF GONADAL AGENESIS

1 reference

12 December 2020

THE XO SYNDROME. A STUDY OF THE DIFFERENTIATED PHENOTYPE IN 25 PATIENTS

1 reference

12 December 2020

AN XY FEMALE WITH ABSENT GONADS AND VESTIGIAL PELVIC ORGANS

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

Chromosome abnormalities in certain diseases of man

1 reference

12 December 2020

Identifiers

0 references

1 reference

28 July 2017

1 reference

PubMed ID

14295659