Triplet repeat expansion mutations: the example of fragile X syndrome.

doi:10.1146/annurev.ne.18.030195.000453

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Triplet repeat expansion mutations: the example of fragile X syndrome.

Annual review of neuroscience - 1 Jan 1995

Warren S T, Ashley C T

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Fragile X Syndrome
Share to Methylation
Share to Mutation
Share to Oligonucleotides

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Pedigree

Share to Repetitive Sequences, Nucleic Acid

Source

Open in PubMed

Identifiers

PMID: 7605075
DOI: 10.1146/annurev.ne.18.030195.000453

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Triplet repeat expansion mutations: the example of fragile X syndrome.PMID 7605075Read ↗

Fragile X: a family of disorders.Semantic proximity Read ↗

[Fragile X syndrome].Semantic proximity Read ↗

[Triplet repeat expansion associated with genetic diseases].Semantic proximity Read ↗

[Fragile X syndrome: a review of diagnosis and treatment].Semantic proximity Read ↗

[Fragile X syndrome: epidemiology, genetics, diagnosis].Semantic proximity Read ↗

Trinucleotide repetition and fragile X syndrome.Semantic proximity Read ↗

[Triple expansion diseases: a new mutational concept].Semantic proximity Read ↗

Clinical conundrums in fragile X syndrome.Semantic proximity Read ↗

Fragile X and other trinucleotide repeat diseases.Semantic proximity Read ↗

DNA structure, mutations, and human genetic disease.Semantic proximity Read ↗

The fragile X syndromes.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.