The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol.

Author:

van Essen A J,Kneppers A L,van der Hout A H,Scheffer H,Ginjaar I B,ten Kate L P,van Ommen G J,Buys C H,Bakker E

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference83 articles.

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2. Carrier detection and prenatal diagnosis of Duchenne/Becker muscular dystrophy (D/BMD) by DNA-analysis. Prog Clin Biol Res;Bakker, E.; Bonten, E.J.; den Dunnen, J.T.,1989

3. Inherit Metab Dis 1989; 12(suppl 34 Voit;T, Neuen Jacob E.

4. Report on the 16th ENMC workshopcarrier diagnosis of Duchenne and Becker muscular a carrier of Becker muscular dystrophy;Abbs, S.; Bobrow, M.;Eur]f Pediatr,1992

5. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman, E.P.; Brown, R.H.; Kunkel, L.M.;Biotechnology,1992

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