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Possibilities and limitations of carrier diagnosis in families with Duchenne muscular dystrophy caused by deletions in the major hot spot region using pulsed-field gel electrophoresis

Item Type:Article
Title:Possibilities and limitations of carrier diagnosis in families with Duchenne muscular dystrophy caused by deletions in the major hot spot region using pulsed-field gel electrophoresis
Creators Name:Huschenbett, J. and Volz, A. and Pfeifer, L. and Speer, A.
Keywords:Agar Gel Electrophoresis, Autoradiography, Chromosome Deletion, DNA, DNA Probes, Exons, Heterozygote Detection, Lymphocytes, Molecular Weight, Muscular Dystrophies, Pedigree, Type II Site-Specific Deoxyribonucleases
Source:Biomedica Biochimica Acta
ISSN:0232-766X
Publisher:Akademie Verl. (Germany)
Volume:50
Page Range:1205-1212
Date:1 January 1991
PubMed:View item in PubMed

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