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Molecular and Clinical Aspects of Angelman Syndrome

โœ Scribed by Dagli, A.; Buiting, K.; Williams, C.A.


Book ID
111871634
Publisher
S. Karger AG
Year
2011
Tongue
English
Weight
619 KB
Volume
0
Category
Article
ISSN
1661-8769

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We analyzed 61 Angelman syndrome (AS) patients by cytogenetic and molecular techniques. On the basis of molecular findings, the patients were classified into the following 4 groups: familial cases without deletion, familial cases with submicroscopic deletion, sporadic cases with deletion, and sporad