Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals-Reference-Cited by-同舟云学术

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

Published:1987-07 Issue:3 Volume:50 Page:509-517
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Koenig M.,Hoffman E.P.,Bertelson C.J.,Monaco A.P.,Feener C.,Kunkel L.M.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference43 articles.

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

2. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs;Bakker;Lancet,1985

3. Screening lambda gt recombinants clones by hybridization to single plaques in situ;Benton;Science,1977

4. Muscular dystrophy in girls with X-autosome translocations;Boyd;J. Med. Genet.,1986

5. Isolation of a cDNA clone from the region of an X:21 translocation that breaks within the Duchenne/Becker muscular dystrophy gene;Burghes;Nature,1987

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