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Article

Identification and regional localization of a highly polymorphic dinucleotide repeat D11S614 to the interval in 11q23.3 flanked by recurrent translocation breakpoints.

Annals of human genetics - 1 Oct 1993

Benham F, Sugiyama R, Hunt D, Gillett G, Smith M

Abstract excerpt

A highly informative dinucleotide repeat polymorphism has been identified at the D11S614 locus on chromosome 11q23. Ten different alleles have been observed at this locus, and the heterozygosity frequency is approximately 85%. Physical localization of this marker in a panel of somatic cell hybrids containing chromosome 11 translocations showed that it maps to 11q23.3, within the interval between the recurrent...

Topics

Alleles
Chromosome Mapping
Chromosomes, Human, Pair 11
Female
Gene Frequency
Genetic Markers
Humans
Hybrid Cells
Male
Polymorphism, Genetic
Repetitive Sequences, Nucleic Acid

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Translocation, Genetic

Source

Identifiers

PMID: 8179290
DOI: 10.1111/j.1469-1809.1993.tb00901.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-8179290-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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Identification and regional localization of a highly polymorphic dinucleotide repeat D11S614 to the interval in 11q23.3 flanked by recurrent translocation breakpoints.PMID 8179290Read ↗

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