Prenatal and carrier detection of Duchenne muscular dystrophy using recombinant DNA technology

Hejtmancik, J. F., Witkowski, J. A., Gunnell, S., Davies, S., Baumbach, L., Caskey, C. T. (1988) Prenatal and carrier detection of Duchenne muscular dystrophy using recombinant DNA technology. In: Nucleic Acid Probes in Diagnosis of Human Genetic Diseases. Wiley, pp. 83-100. ISBN 9780471500353

URL: http://books.google.com/books?id=W1iPAAAACAAJ
Item Type: Book Section
Subjects: bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification
diseases & disorders > congenital hereditary genetic diseases > muscular dystrophy
bioinformatics > genomics and proteomics > genetics & nucleic acid processing > DNA, RNA structure, function, modification > recombination
CSHL Authors:
Communities: Banbury Center
Depositing User: Matt Covey
Date: 1988
Date Deposited: 02 Dec 2014 21:45
Last Modified: 02 Dec 2014 21:45
URI: http://repository.cshl.edu/id/eprint/30367

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