(Q34633953)

3 August 2017

Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome (English)

1 reference

3 August 2017

Hecht F

1

1 reference

3 August 2017

Jones DL

series ordinal

2

1 reference

3 August 2017

Delay M

series ordinal

3

1 reference

3 August 2017

Klevit H

series ordinal

4

1 reference

3 August 2017

language of work or name

English

0 references

publication date

1 March 1970

1 reference

Journal of Medical Genetics

3 August 2017

1 reference

3 August 2017

7

1 reference

3 August 2017

1-4

1 reference

3 August 2017

1

1 reference

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

3 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468913

Apparent deletion of X chromosome in a prepuberal girl

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468913

Statistical analysis of the normal human karyotype

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468913

Structural abnormalities of the sex chromosomes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468913

On a case of XXdc ovarian dysgenesis

7 July 2018

1 reference

12 December 2020

Cytogenetic studies in primary amenorrhoea

1 reference

12 December 2020

A NOTE ON THE MEAN MEASUREMENTS OF HUMAN CHROMOSOMES

1 reference

12 December 2020

OVARIAN DYSGENESIS DUE TO DELETION OF THE X CHROMOSOME

1 reference

12 December 2020

Identifiers

PMCID

1468913

1 reference

3 August 2017

1 reference