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Article

Fragile x-associated premature ovarian failure in a large Turkish cohort: Findings of Hacettepe Fragile X Registry.

European journal of obstetrics, gynecology, and reproductive biology - 1 Feb 2018

Utine Gülen Eda, Şimşek-Kiper Pelin Özlem, Akgün-Doğan Özlem, Ürel-Demir Gizem, Alanay Yasemin, Aktaş Dilek, Boduroğlu Koray, Tunçbilek Ergül, Alikaşifoğlu Mehmet

Abstract excerpt

OBJECTIVE: To determine frequency of fragile X associated premature ovarian insufficiency (FXPOI) among Turkish premutation carriers. STUDY DESIGN: FMR1 premutation is the single most common genetic cause of POI (FXPOI). Fragile X Registry at Hacettepe University has been reviewed for the frequency of FXPOI among female premutation carriers. Since 1991 when FMR1 testing was available, 760 individuals from 243...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 29275276
DOI: 10.1016/j.ejogrb.2017.12.028

Genes

FMR1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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