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Article

Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects.

Annals of clinical biochemistry - 1 Sept 1997

Chen T A, Lu X F, Che P K, Ho W K

Abstract excerpt

The fragile X syndrome is believed to be caused by an expansion of a CGG trinucleotide repeat segment in the FMR-1 gene on the fragile X site of the long arm of the X-chromosome. To understand the variation of the CGG repeat in the FMR-1 gene in southern Chinese from the Hong Kong and Guangzhou area, we undertook the present study. A total of 83 normal and three fragile X subjects were examined. In the normal...

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PMID: 9293305
DOI: 10.1177/000456329703400504

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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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