Startling mosaicism of the Y-chromosome and tandem duplication of the SRY and DAZ genes in patients with Turner Syndrome (Q33386810)

26 July 2017

title

Startling mosaicism of the Y-chromosome and tandem duplication of the SRY and DAZ genes in patients with Turner Syndrome (English)

1 reference

26 July 2017

1 reference

Sanjay Premi

1

1 reference

26 July 2017

Jyoti Srivastava

series ordinal

2

1 reference

26 July 2017

Ganesan Panneer

series ordinal

3

1 reference

26 July 2017

Sher Ali

series ordinal

4

1 reference

26 July 2017

language of work or name

English

0 references

publication date

24 November 2008

1 reference

26 July 2017

1 reference

26 July 2017

volume

3

1 reference

26 July 2017

issue

11

1 reference

26 July 2017

page(s)

e3796

1 reference

Creative Commons Attribution 4.0 International

26 July 2017

copyright license

start time

24 November 2008

1 reference

April 2022 Public Data File from Crossref

0 references

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2582957

Occurrence of gonadoblastoma in females with Turner syndrome and Y chromosome material: a population study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2582957

Four DAZ genes in two clusters found in the AZFc 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=2582957

Discordant phenotypes and 45,X/46,X,idic(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=2582957

Pathogenetics of 45,X/46,XY gonadal 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=2582957

45,X/46,X,idic(Yq) mosaicism: clinical, cytogenetic, and molecular studies in four individuals

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2582957

Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed 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=2582957

Isodicentric Y chromosome: cytogenetic, molecular and clinical studies 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=2582957

Cytogenetic and molecular analysis of sex-chromosome monosomy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2582957

Exclusion of chromosomal mosaicism: tables of 90%, 95% and 99% confidence limits and comments on use

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2582957

Turner syndrome: a cytogenetic and molecular study

21 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003796

A comparative study between infertile males and patients with Turner syndrome to determine the influence of sex chromosome mosaicism and the breakpoints of structurally abnormal Y chromosomes on phenotypic sex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003796

Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003796

AZFc somatic microdeletions and copy number polymorphism of the DAZ genes in human males exposed to natural background radiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003796

Epidemiological, endocrine and metabolic features in Turner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003796

Fate of SRY, PABY, DYS1, DYZ3 and DYZ1 loci in Indian patients harbouring sex chromosomal anomalies

21 January 2018

1 reference

12 December 2020

Problems of detecting mosaicism in skin. A case of trisomy 8 mosaicism illustrating the advantages of in situ tissue culture

1 reference

12 December 2020

1 reference

12 December 2020

Tandem duplication and copy number polymorphism of the SRY gene in patients with sex chromosome anomalies and males exposed to natural background radiation

1 reference

12 December 2020

Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses

1 reference

12 December 2020

DNA finger printing by oligonucleotide probes specific for simple repeats

1 reference

12 December 2020

Detection of Turner syndrome using high-throughput quantitative genotyping

1 reference

12 December 2020

Occurrence of Gonadoblastoma in Females with Turner Syndrome and Y Chromosome Material: A Population Study1

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0003796

Identifiers

DOI

1 reference

26 July 2017

0 references

1 reference

26 July 2017

1 reference