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Article

Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic.

American journal of medical genetics - 28 May 1999

Pekarík V, Blazková M, Kozák L

Abstract excerpt

We report on the haplotype analysis with polymorphic repeat markers DXS548 and FRAXAC1 next to the FMR1 gene in 37 unrelated fragile X and 36 control chromosomes from Bohemia and Moravia. Our results suggest a significant linkage disequilibrium between fragile X mutations and certain DXS548-FRAXAC1 haplotypes. Allele frequencies obtained differ slightly from those of other European populations with allele 194...

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Source

Identifiers

PMID: 10331594
DOI: 10.1002/(sici)1096-8628(19990528)84:3<214::aid-ajmg9>3.3.co;2-1

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic.PMID 10331594Read ↗

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Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.Semantic proximity Read ↗

Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X alleles.Semantic proximity Read ↗

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