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. Nucleic Acid Probes in Diagnosis of Human Genetic Diseases. pp. 83-100.
Item Type: | Paper |
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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: | 05 Oct 2021 12:08 |
URI: | https://repository.cshl.edu/id/eprint/30367 |
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