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Prenatal deletion detection in a sporadic case of Duchenne muscular dystrophy without genotype information from the affected individual

✍ Scribed by F. Peinemann; M. Wagner; U. Franke; M. Kulle; J. Reiss


Publisher
Springer
Year
1991
Tongue
English
Weight
509 KB
Volume
150
Category
Article
ISSN
0340-6997

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