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Article

A linkage map of microsatellite markers on the human X chromosome.

Genomics - 1 Apr 1994

Donnelly A, Kozman H, Gedeon A K, Webb S, Lynch M, Sutherland G R, Richards R I, Mulley J C

Abstract excerpt

The efficiency of mapping and diagnosis of X-linked disorders by linkage depends upon the existence of a high-density genetic map of polymerase chain reaction (PCR)-based markers. DXS1120, DXS1122, DXS1123, DXS1124, DXS1125, DXS1126, and DXS1153 were randomly isolated from a flow-sorted lambda ba...

Topics

Alleles
Base Sequence
Chromosome Mapping
Chromosomes, Human
DNA Primers
DNA, Satellite
Gene Library
Genetic Linkage
Genetic Markers
Heterozygote
Humans
Molecular Sequence Data

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Mutation

Odds Ratio

Polymerase Chain Reaction

Repetitive Sequences, Nucleic Acid

X Chromosome

Source

Identifiers

PMID: 8034308
DOI: 10.1006/geno.1994.1189

Genes

ALAS2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8034308-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

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

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Click a neighbor to travelStep 1 · 12 closest

A linkage map of microsatellite markers on the human X chromosome.PMID 8034308Read ↗

Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28.Semantic proximity Read ↗

Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome.Semantic proximity Read ↗

A high-density single-nucleotide polymorphism map of Xq25-q28.Semantic proximity Read ↗

Genome analysis and the human X chromosome.Semantic proximity Read ↗

A multipoint linkage map of the distal short arm of the human X chromosome.Semantic proximity Read ↗

A high-density SNP map for the FRAX region of the X chromosome. Single-nucleotide polymorphisms.Semantic proximity Read ↗

The STR cluster DXS10148-DXS8378-DXS10135 provides a powerful tool for X-chromosomal haplotyping at Xp22.Semantic proximity Read ↗

Four STR polymorphisms map to a 500 kb region between DXS15 and DXS134.Semantic proximity Read ↗

Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.Semantic proximity Read ↗

Validation of the X-chromosomal STR DXS6809.Semantic proximity Read ↗

The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13).Semantic proximity Read ↗

Sequence structure and population data of two X-linked markers: DXS7423 and DXS8377.Semantic proximity Read ↗

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