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Article

Identification of new markers in Xp21 between DXS28 (C7) and DMD.

Genomics - 1 Aug 1992

Worley K C, Towbin J A, Zhu X M, Barker D F, Ballabio A, Chamberlain J, Biesecker L G, Blethen S L, Brosnan P, Fox J E

Abstract excerpt

Characterization of Xp21 distal to Duchenne muscular dystrophy (DMD) in the region containing the genes for adrenal hypoplasia congenita (AHC) and glycerol kinase deficiency (GKD) has been limited due to a paucity of probes. Two probes were localized between DXS28 (C7) and AHC, the yeast artificial chromosome insert YHX39 (DXS727) and the polymorphic phage clone QST59 (DXS319). A genomic clone, FT1 (DXS726), 3'...

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Source

Identifiers

PMID: 1505987
DOI: 10.1016/0888-7543(92)90007-f

Genes

DMD

Provenance

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of new markers in Xp21 between DXS28 (C7) and DMD.PMID 1505987Read ↗

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 rare MspI RFLP of the DMD probe p20 (DXS269).Semantic proximity Read ↗

A new polymorphic probe on chromosome 22q (XD6) (D22S313).Semantic proximity Read ↗

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions.Semantic proximity Read ↗

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

Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophy.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 ↗

Three novel mutations and a de novo deletion mutation of the DAX-1 gene in patients with X-linked adrenal hypoplasia congenita.Semantic proximity Read ↗

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment.Semantic proximity Read ↗

Primers for the dinucleotide repeat at the DXS453 locus also recognizes the DXS983 locus.Semantic proximity Read ↗

Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene.Semantic proximity Read ↗

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