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Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophy
- Correspondence to: Dr M F Buckley Director of Laboratory Genetics, South Eastern Area Laboratory Services, Prince of Wales Hospital, High Street, Randwick NSW 2031, Sydney, Australia; michael.buckley{at}sesiahs.health.nsw.gov.au
Citation
Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophy
Publication history
- Received November 3, 2006
- Accepted January 19, 2007
- Revised January 3, 2007
- First published January 26, 2007.
Online issue publication
April 27, 2016
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Copyright 2007 Journal of Medical Genetics