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Article

Analysis of FMR1 gene premutation and X chromosome cytogenetic abnormalities in 100 Tunisian patients presenting premature ovarian failure.

Annales d'endocrinologie - 1 Dec 2015

Bouali Nouha, Hmida Dorra, Mougou Soumaya, Bouligand Jérôme, Lakhal Besma, Dimessi Sarra, Francou Bruno, Saad Ghada, Trabelsi Saoussen, Zaouali Monia, Gribaa Moez, Chaieb Molka, Bibi Mouhamed, Guiochon-Mantel Anne, Saad Ali

Abstract excerpt

OBJECTIVE: To evaluate the prevalence of FMR1 premutations and X chromosome cytogenetic abnormalities in a large cohort of Tunisian women with premature ovarian failure (POF). PATIENTS AND METHODS: The cohort consisted of 127 Tunisian women with POF referred by endocrinologists and gynecologists for genetic investigation in the context of idiopathic POF and altered hormonal profiles. Clinical information...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Fragile X Mental Retardation Protein

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Source

Identifiers

PMID: 26593861
DOI: 10.1016/j.ando.2015.10.001

Genes

FMR1

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.

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