Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115.

Author:

Passos-Bueno M R,Rapaport D,Love D,Flint T,Bortolini E R,Zatz M,Davies K E

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference27 articles.

1. Duchenne muscular dystrophy;Emery, A.E.H.,1987

2. Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences;Kingston, H.M.; Sarfarazi, M.; Thomas, T.; Harper, P.S.;Hum Genet,1984

3. Determination of the 'power' of therapeutic trials based on the natural history;Muscle Nerve,1983

4. An X autosome translocation in a girl with Duchenne muscular dystrophy (DMD): evidence for DMD gene localisation;Greenstein, R.M.; Reardon, M.P.; Chan, T.S.;Pediatr Res,1977

5. Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm;Lindenbaum, R.H.; Clarke, G.; Patel, C.; Moncrieff, M.; Hughes, J.T.;J Med Genet,1979

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