Becker muscular dystrophy: correlation of deletion type with clinical severity.

Author:

Norman A M,Thomas N S,Kingston H M,Harper P S

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference16 articles.

1. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals;Koenig, M.; Hoffman, E.P.; Bertelson, C.J.; Monaco, A.P.; Feener, C.; Kunkel, L.M.;Cell,1987

2. Dystrophin: the protein product of the Duchenne muscular dystrophv locus;Hoffman, E.P.; Brown, R.H.; Kunkel, L.M.;Cell,1987

3. An explanation for the phenotvpic differences between patients bearing partial deletions of the DMD locus;Monaco, A.P.; Bertelson, C.J.; Liechti-Gallati, S.; Moser, H.; Kunkel, L.M.;Genomics,1988

4. Effective strategy for the prenatal prediction of Duchenne and Becker muscular dystrophy;Forrest, S.M.; Smith, T.J.; Cross, G.S.;Lancet,1987

5. Preferential deletion of exons in Duchenne and Becker muscular dystrophies;Forrest, S.M.; Cross, G.S.; Speer, A.; Gardner-Medwin, D.; Burn, J.; Davies, K.E.;Nature,1987

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