Molecular genetic analysis of the 3p- syndrome.

doi:10.1093/hmg/3.6.903

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Article

Molecular genetic analysis of the 3p- syndrome.

Human molecular genetics - 1 Jun 1994

Phipps M E, Latif F, Prowse A, Payne S J, Dietz-Band J, Leversha M, Affara N A, Moore A T, Tolmie J, Schinzel A

Abstract excerpt

Molecular genetic analysis of five cases of 3p- syndrome (del(3)(qter-->p25:)) was performed to investigate the relationship between the molecular pathology and clinical phenotype. Fluorescence in situ hybridization studies and analysis of polymorphic DNA markers from chromosome 3p25-p26 demonstr...

Topics

Abnormalities, Multiple
Adult
Cell Line
Child
Chromosome Deletion
Chromosome Mapping
Chromosomes, Human, Pair 3
Female
Follow-Up Studies
Genetic Markers
Humans
In Situ Hybridization, Fluorescence
Infant
Lymphocytes
Male
Phenotype
Polymorphism, Genetic
Syndrome

Source

Open in PubMed

Identifiers

PMID: 7951234
DOI: 10.1093/hmg/3.6.903

Genes

VHL
RAF1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-7951234-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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