Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

PloS one - 1 Jan 2008

Premi Sanjay, Srivastava Jyoti, Panneer Ganesan, Ali Sher

Abstract excerpt

Presence of the human Y-chromosome in females with Turner Syndrome (TS) enhances the risk of development of gonadoblastoma besides causing several other phenotypic abnormalities. In the present study, we have analyzed the Y chromosome in 15 clinically diagnosed Turner Syndrome (TS) patients and detected high level of mosaicisms ranging from 45,XO:46,XY = 100:0% in 4; 45,XO:46,XY:46XX = 4:94:2 in 8; and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosomes, Human, Y
Share to Cytogenetic Analysis
Share to Genes, sry

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mosaicism

Share to Sex Chromosome Aberrations

Share to Tandem Repeat Sequences

Share to Turner Syndrome

Share to Uterus

Source

Open in PubMed Open full text

Identifiers

PMID: 19030103
DOI: 10.1371/journal.pone.0003796
PMCID: PMC2582957

Genes

SRY
CDY1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Startling mosaicism of the Y-chromosome and tandem duplication of the SRY and DAZ genes in patients with Turner Syndrome.PMID 19030103Read ↗

Mutational landscape of the human Y chromosome-linked genes and loci in patients with hypogonadism.Semantic proximity Read ↗

SRY Gene Increases the Risk of Developing Gonadoblastoma and/or Nontumoral Gonadal Lesions in Turner SyndromeSemantic proximity Read ↗

[Analysis of specific sequences in female patients with Turner syndrome--initial study].Semantic proximity Read ↗

A SRY-HMG box frame shift mutation inherited from a mosaic father with a mild form of testicular dysgenesis syndrome in Turner syndrome patientSemantic proximity Read ↗

Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive.Semantic proximity Read ↗

Analysis of Turner syndrome patients within the Jordanian population, with a focus on four patients with Y chromosome abnormalities.Semantic proximity Read ↗

SRY-positive 45,X/46,XY karyotype in a phenotypically Turner-like Chinese adolescent female with ovarian dysgerminoma and gonadoblastoma.Semantic proximity Read ↗

Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients.Semantic proximity Read ↗

Y chromosome in Turner syndrome: review of the literatureSemantic proximity Read ↗

[Y chromosome in Turner syndrome].Semantic proximity Read ↗

Analysis of the sex-determining region of the Y chromosome (SRY) in sex reversed patients: point-mutation in SRY causing sex-reversion in a 46,XY female.Semantic proximity Read ↗

Molecular basis of mammalian sexual determination: activation of Mullerian inhibiting substance gene expression by SRYSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.