DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysis-Reference-Cited by-同舟云学术

DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysis

Published:1990-07 Issue:3 Volume:7 Page:442-444
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Towbin Jeffrey A.,Chamberlain Jeffrey S.,Wu Darong,Pillers De Ann M.,Seltzer William K.,McCabe Edward R.B.

Publisher

Elsevier BV

Subject

Genetics

Reference21 articles.

1. A strategy to reveal high frequency RFLPs along the human X chromosome;Aldridge;Amer. J. Hum. Genet,1984

2. A Xp21 deletion assigns locus DXS 28 (C7) proximal to DXS 68 (L1.4) and DXS 67 (B24) and has its proximal breakpoint in the first exon of dystrophin-8;Bartley;Pediatr. Res,1989

3. Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy;Boyd;Clin. Genet,1986

4. Long range restriction map around the Duchenne muscular dystrophy gene;Burmeister;Nature (London),1986

5. A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene;Burmeister;Genomics,1988

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2. Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome;American Journal of Medical Genetics;1993-11-15

3. Negative-Configuration Electroretinogram in Oregon Eye Disease;Archives of Ophthalmology;1993-11-01

4. Isolation of the human Xp21 glycerol kinase gene by positional cloning;Human Molecular Genetics;1993

5. A case of myopathy associated with a dystrophin gene deletion and abnormal glycogen storage;Muscle & Nerve;1993-01