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Article

A molecular and cytogenetic investigation of FMR1 gene premutations in Polish patients with primary ovarian insufficiency.

European journal of obstetrics, gynecology, and reproductive biology - 1 Apr 2011

Rajkiewicz Marta, Szlendak-Sauer Katarzyna, Sulek Anna, Gawlik-Zawislak Sylwia, Krysa Wioletta, Radowicki Stanislaw, Zaremba Jacek

Abstract excerpt

OBJECTIVE: The aim of this study was to determine the prevalence of premutations in the FMR1 gene that cause primary ovarian insufficiency (POI) in a group of affected women. STUDY DESIGN: Forty DNA samples were purified from peripheral blood collected from women with ovarian failure who were und...

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Share to Blood Cells
Share to Chromosomes, Human, X
Share to Cytogenetic Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fragile X Mental Retardation Protein

Share to Fragile X Syndrome

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Share to Primary Ovarian Insufficiency

Share to Translocation, Genetic

Source

Identifiers

PMID: 21276648
DOI: 10.1016/j.ejogrb.2010.12.031

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21276648-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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