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Article

Analysis of FMR1 (CGG)n alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia.

European journal of human genetics : EJHG - 1 Jan 2000

Larsen L A, Armstrong J S, Grønskov K, Hjalgrim H, Brøndum-Nielsen K, Hasholt L, Nørgaard-Pedersen B, Vuust J

Abstract excerpt

The fragile X syndrome is caused by the expansion of a polymorphic (CGG)n tract in the promoter region of the FMR1 gene. Apparently the incidence of fragile X syndrome is rare in the population of Greenland. In order to examine population-related factors involved in stability of the (CGG)n sequence, DNA samples obtained randomly from the Greenlandic population were analysed for size and AGG interspersion pattern...

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Identifiers

PMID: 10573009
DOI: 10.1038/sj.ejhg.5200374

Genes

FMR1

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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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Analysis of FMR1 (CGG)n alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia.PMID 10573009Read ↗

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