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Article

The fragile X CGG repeat shows a marked level of instability in hereditary non-polyposis colorectal cancer patients.

European journal of human genetics : EJHG - 1 Jan 2000

Fulchignoni-Lataud M C, Olchwang S, Serre J L

Abstract excerpt

The allelic variation of the FMR1 CGG repeat was investigated by small-pool PCR in nonneoplastic peripheral blood leukocytes from HNPCC patients and matched controls for similar CGG repeat lengths. The allelic variation for repeat lengths appears to be roughly twice as frequent in HNPCC patients...

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Identifiers

PMID: 9195158

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-9195158-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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Research trail→

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The fragile X CGG repeat shows a marked level of instability in hereditary non-polyposis colorectal cancer patients.PMID 9195158Read ↗

Microsatellite instability in the peripheral blood leukocytes of HNPCC patients.Semantic proximity Read ↗

Analysis of germline variation at the FMR1 CGG repeat shows variation in the normal-premutated borderline range.Semantic proximity Read ↗

Is Low FMR1 CGG Repeat Length in Males Correlated with Family History of BRCA-Associated Cancers? An Exploratory Analysis of Medical Records.Semantic proximity Read ↗

Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic mice.Semantic proximity Read ↗

CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles.Semantic proximity Read ↗

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

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

CGG repeat in the FMR1 gene: size matters.Semantic proximity Read ↗

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