DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.

Author:

Bakker E,Bonten E J,De Lange L F,Veenema H,Majoor-Krakauer D,Hofker M H,Van Ommen G J,Pearson P L

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference22 articles.

1. Review of studies on the proportion and origin of new mutants in Duchenne muscular dystrophy;Moser, H.,1984

2. Serum creatine kinase activity and carrier status for Duchenne muscular dystrophy;Bullock, D.G.; McSweeny, F.M.; Whitehead, T.P.; Edwards, J.H.;Lancet,1979

3. Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X-chromosome;Davies, K.E.; Pearson, P.L.; Harper, P.S.;Nucleic Acids Res,1983

4. A strategy to reveal high frequency RFLPs along the human chromosome;Aldridge, J.; Kunkel, L.M.; Bruns, G.;Am J Hum Genet; Isolation of probes detecting RFLPs from X-chromosome specific libraries: potential use for diagnosis of Duchenne muscular dystrophy,1984

5. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs;Bakker, E.; Hofker, M.H.; Goor, N.;Lancet,1985

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