Molecular deletion patterns in Duchenne and Becker type muscular dystrophy-Reference-Cited by-同舟云学术

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Molecular deletion patterns in Duchenne and Becker type muscular dystrophy

Published:1989-03 Issue:4 Volume:81 Page:343-348
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Liechti-Gallati S.,Koenig M.,Kunkel L. M.,Frey D.,Boltshauser E.,Schneider V.,Braga S.,Moser H.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00283688.pdf

Reference41 articles.

1. Akita Y, Ohno S, Goto J, Nakano J, Takatsu M, Sugita H, Suzuki K (1987) Diagnosis of Duchenne and Becker muscular dystrophies by DNA polymorphisms. Jpn J Hum Genet 32:71–82

2. Bartlett RJ, Pericak-Vance MA, Koh J, Yamaoka L, Chen JK, Hung WY, Speer MC, Wapenaar MC, Van Ommen GJB, Bakker E, Pearson PL, Kandt RS, Siddique T, Gilbert JR, Lee JE, Sirotkin-Roses MJ, Roses AD (1988) Duchenne muscular dystrophy: high frequency of deletions. Neurology 38:1–4

3. Bartley JA, Patil S, Davenport S, Goldstein D, Pickens J (1986) Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion. J Pediatr 108:189–192

4. Bertelson CJ, Bertley JA, Monaco AP, Colleti-Feener C, Fishbeck K, Kunkel LM (1986) Localization of Xp21 meiotic exchange points in Duchenne muscular dystrophy families. J Med Genet 23: 531–537

5. Boyd Y, Buckle V, Holt S, Munro E, Hunter D, Craig I (1986) Muscular dystrophy in girls with X-autosome translocations. J Med Genet 23:484–490

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