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Article

Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation.

Journal of neurogenetics - 1 Jan 2000

Major Tamara, Culjkovic Biljana, Stojkovic Oliver, Gucscekic Marija, Lakic Aneta, Romac Stanka

Abstract excerpt

Mutations at two fragile sites, FRAXA and FRAXE, loci are caused by an expansion of a CGG/GCC trinucleotide repeat and are characterized by mental retardation. Here we report molecular screening survey of 97 unrelated individuals diagnosed with non-specific mental retardation (MR), which produced positive test for FRAXA in two boys and none positive for the FRAXE mutation. In addition, we studied allelic...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 14668200
DOI: 10.1080/neg.17.2-3.223.230

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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Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation.PMID 14668200Read ↗

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