Some studies of the duchenne and autosomal recessive types of muscular dystrophy

Author:

Gardner-Medwin David,Sharpies Peta

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference28 articles.

1. Progressive muscular dystrophy of the Duchenne type in a young girl associated with an aberration of chromosome X;Verellen,1977

2. Linkage relationship of a cloned DNA sequence on the short arm of the X-chromosome to Duchenne muscular dystrophy;Murray;Nature,1982

3. Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X-chromosome;Kingston;J Med Genet,,1983

4. Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa and McLeod syndrome;Francke;Am J Hum Genet,1985

5. Specific cloning of DNA fragments absent from the DNA of a male patient with an X-chromosome deletion;Kunkel;Proc Nat Acad Sci,1985

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