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Article

A study on the role of FMR1 CGG trinucleotide repeats in Jordanian poor ovarian responders.

Gene - 30 Jan 2021

Batiha Osamah, Shaaban Sherin T, Al-Smadi Mohammad, Jarun Yousef, Maswadeh Ahmad, Alahmad Nour Alhoda, Al-Talib Mohammad M

Abstract excerpt

The expansion of trinucleotide CGG repeats in the promoter of fragile X mental retardation 1 (FMR1) gene is associated with fragile X and fragile X associated tremor/ataxia syndromes. While the expansion of CGG repeats has been associated with such neuro/psychiatric diseases, the contraction of CGG repeats has been recently suggested as an indication of ovarian dysfunction. This study aimed to evaluate a possible...

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Identifiers

PMID: 33007370
DOI: 10.1016/j.gene.2020.145174

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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.

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