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Comment: How many are too many when discussing triplet repeats in the FMR1 gene and the Fragile X syndrome?

Genetic testing - 1 Jan 2001

Gilbert F

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Share to Fragile X Mental Retardation Protein
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 11551101
DOI: 10.1089/109065701753145619

Genes

FMR1

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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Click a neighbor to travelStep 1 · 12 closest

Comment: How many are too many when discussing triplet repeats in the FMR1 gene and the Fragile X syndrome?PMID 11551101Read ↗

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Triplet repeat expansion mutations: the example of fragile X syndrome.Semantic proximity Read ↗

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Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand?Semantic proximity Read ↗

Non-CGG trinucleotide repeat expansions as pathogenic genetic mutations in Fragile X SyndromeSemantic proximity Read ↗

The fragile-X syndrome after the discovery of the FMR-1 gene. The clinical geneticist faced with the unravelled enigmas and persisting difficulties in genetic counseling.Semantic proximity Read ↗

Insight and Recommendations for Fragile X Premutation Associated Conditions from the 5th International Conference on <em>FMR1</em> PremutationSemantic proximity Read ↗

A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype.Semantic proximity Read ↗

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Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.Semantic proximity Read ↗

Apparent FMR1 allele instability in non-fragile X males.Semantic proximity Read ↗

Complex behavior of simple repeats: the fragile X syndrome.Semantic proximity Read ↗

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