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Article

The detection of a VNTR at the Huntington disease genetic marker D4S10.

Human molecular genetics - 1 Jul 1993

Carlock L, Vo T

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Identifiers

PMID: 8364554
DOI: 10.1093/hmg/2.7.1079

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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.

Related research

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

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The detection of a VNTR at the Huntington disease genetic marker D4S10.PMID 8364554Read ↗

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Huntington disease in Finland: a molecular and genealogical study.Semantic proximity Read ↗

Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat number.Semantic proximity Read ↗

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group.Semantic proximity Read ↗

Dinucleotide repeat polymorphism at the D4S251 locus.Semantic proximity Read ↗

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