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Article

Simple molecular diagnostic method for fragile X syndrome in Egyptian patients: pilot study.

Acta biochimica Polonica - 1 Jan 2014

Meguid Nagwa A, Ismail Manal F, El-Mahdy Rasha S, Barakat Maged A, El-Awady Mostafa K

Abstract excerpt

BACKGROUND: Poor knowledge about Fragile X syndrome (FXS) may be a major barrier to early diagnosis that could improve quality of life and prognosis especially in the developing countries. AIM: The aim of this study was to evaluate simple and reproducible method for premutation detection in females of fragile X families for the first time in Egypt. SUBJECTS AND METHODS: We have developed a rapid modified...

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Source

Identifiers

PMID: 24936518

Genes

FMR1

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.

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