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De Novo Rearrangements Found in 2% of Index Patients with Spinal Muscular Atrophy: Mutational Mechanisms, Parental Origin, Mutation Rate, and Implications for Genetic Counseling

✍ Scribed by Brunhilde Wirth; Thorsten Schmidt; Eric Hahnen; Sabine Rudnik-Schöneborn; Michael Krawczak; Bertram Müller-Myhsok; Jutta Schönling; Klaus Zerres


Book ID
117852209
Publisher
American Society of Human Genetics
Year
1997
Tongue
English
Weight
188 KB
Volume
61
Category
Article
ISSN
0002-9297

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