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Article

Genetic diversity at the FMR1 locus in Mexican population.

Archives of medical research - 1 Jan 2000

Rosales-Reynoso Mónica Alejandra, Mendoza-Carrera Francisco, Troyo-Sanromán Rogelio, Medina Claudina, Barros-Núñez Patricio

Abstract excerpt

BACKGROUND: Fragile X syndrome is the most frequent cause of inherited mental retardation; it is caused by expansion of CGG repeats in the first exon of the FMR1 gene. Number of CGG repeats varies between 6 and 50 triplets in normal individuals and the most common alleles have 29 or 30 repeats. Allelic patterns in the global population are similar; however, some reports show statistical differences among several...

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Identifiers

PMID: 15950084
DOI: 10.1016/j.arcmed.2004.05.005

Genes

FMR1

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Genetic diversity at the FMR1 locus in Mexican population.PMID 15950084Read ↗

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Allele distribution at the FMR1 locus in the general Chinese population.Semantic proximity Read ↗

CGG repeat expansion at FMR1 locus - A new molecular diagnostic algorithm in fragile X syndrome.Semantic proximity Read ↗

Reduction in the number of CGG repeats on the FMR1 gene in carriers of genetic disorders versus noncarriers.Semantic proximity Read ↗

FMR1 allele frequencies in 51,000 newborns: a large-scale population study in China.Semantic proximity Read ↗

Fragile X syndrome: the FMR1 CGG repeat distribution among world populations.Semantic proximity Read ↗

[Analysis of AGG interspersion of the FMR1 gene in fragile X syndrome].Semantic proximity Read ↗

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