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Article

Molecular analysis of fragile X syndrome in Antalya Province.

Indian journal of medical sciences - 1 Apr 2005

Bilgen T, Keser I, Mihci E, Haspolat S, Tacoy S, Luleci G

Abstract excerpt

BACKGROUND: Detection of the (CGG)n repeats in the FMR1 gene that cause the fragile X syndrome (FXS), has become a milestone for phenotype-genotype correlation in FXS. AIMS: To screen the FMR1 gene CGG repeats in index cases with FXS and their family members in the Antalya Province. SETTING AND DESIGN: This study was prospectively conducted between January 2000 and March 2005 in Department of Medical Biology and...

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Source

Identifiers

PMID: 15876779

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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