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Article

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

Genomics - 1 Oct 1992

Porteous M E, Curtis A, Lindsay S, Williams O, Goudie D, Kamakari S, Bhattacharya S S

Abstract excerpt

Aarskog syndrome has been mapped to Xq13 on the basis of a patient carrying an Xq13:8p21.2 translocation. We have identified a new microsatellite marker in a clone mapping to this region (HX60;DXS566). Using primers flanking this microsatellite along with primers detecting a microsatellite at PGK1P1 and DXS255, and DXS72, we have performed a multipoint analysis in a large kindred with Aarskog syndrome. Our...

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Identifiers

PMID: 1427846
DOI: 10.1016/s0888-7543(05)80219-8

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13).PMID 1427846Read ↗

Homologous loci DXYS156X and DXYS156Y contain a polymorphic pentanucleotide repeat (TAAAA)n and map to human X and Y chromosomes.Semantic proximity Read ↗

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

A linkage map of microsatellite markers on the human X chromosome.Semantic proximity Read ↗

Dinucleotide polymorphism at the DXS1178 locus is tightly linked to PGK1 at Xq13.Semantic proximity Read ↗

Identification of new markers in Xp21 between DXS28 (C7) and DMD.Semantic proximity Read ↗

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

YAC/STS map of 15Mb of Xp21.3-p11.3, at 100kb resolution, with refined comparisons of genetic distances and DMD structure.Semantic proximity Read ↗

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

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

X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markers.Semantic proximity Read ↗

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