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

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

Casopis lekaru ceskych - 1 Jul 2002

Vodicka R, Vrtĕl R, Adamová K, Zapletalová J, Lebl J, Santavý J, Santavá A, Kolárová J, Konvalinka D, Krejciríková E

Abstract excerpt

BACKGROUND: DNA sequences from chromosome Y can cause gonadoblastoma development in patients with Turner syndrome (TS). Estimated risk is about 30%. The aim of the study is detection of Y-sequences of DNA level, calculation of mosaicism and its cytogenetic location. Clinical result of the study is the recommendation to gonadectomy of proved positive patients. METHODS AND RESULTS: Samples from 110 patients were...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to SRY gene
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to In Situ Hybridization, Fluorescence

Share to Polymerase Chain Reaction

Share to Sequence Analysis, DNA

Share to Turner Syndrome

Share to Y Chromosome

Source

Identifiers

PMID: 12238030

Genes

SRY

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Analysis of specific sequences in female patients with Turner syndrome--initial study].PMID 12238030Read ↗

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

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

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

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

Y chromosome in Turner syndrome: detection of hidden mosaicism and the report of a rare X;Y translocation case.Semantic proximity Read ↗

[Turner syndrome in a girl with marker chromosome in karyotype].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 ↗

The Use of Fluorescence In situ Hybridisation in the Diagnosis of Hidden Mosaicism in Egyptian Patients with Turner SyndromeSemantic proximity Read ↗

PCR detection of Y-specific sequences in patients with Ullrich-Turner syndrome: clinical implications and limitations.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 ↗

[Frequency of prevalence of Turner syndrome in fetuses of patients referred to genetic amniocentesis in 2007-2011].Semantic proximity Read ↗

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