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Article

Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions.

Human molecular genetics - 1 Dec 1995

Eichler E E, Hammond H A, Macpherson J N, Ward P A, Nelson D L

Abstract excerpt

Both sequence length and sequence content are important parameters in determining stability of the fragile X syndrome CGG repeat. In order to estimate the incidence of uninterrupted CGG repeats in the general population and to gain insight into mechanisms responsible for the loss and acquisition...

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Source

Identifiers

PMID: 8634688
DOI: 10.1093/hmg/4.12.2199

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-8634688-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions.PMID 8634688Read ↗

Length of uninterrupted CGG repeats determines instability in the FMR1 gene.Semantic proximity Read ↗

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The role of AGG interruptions in the transcription of FMR1 premutation alleles.Semantic proximity Read ↗

FMR1 CGG repeat patterns and flanking haplotypes in three Asian populations and their relationship with repeat instability.Semantic proximity Read ↗

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

AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome.Semantic proximity Read ↗

Fragile X "gray zone" alleles: AGG patterns, expansion risks, and associated haplotypes.Semantic proximity Read ↗

FMR1 in global populations.Semantic proximity Read ↗

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