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Molecular cytogenetics of Prader-Willi and Angelman syndromes

✍ Scribed by Butler, MerlinG.; Greenstein, MarkA.


Book ID
123475028
Publisher
The Lancet
Year
1991
Tongue
English
Weight
162 KB
Volume
338
Category
Article
ISSN
0140-6736

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## Abstract The majority of patients with Angelman syndrome and Prader‐Willi syndrome have a cytogenetic and molecular deletion of chromosome 15q11q13 with the primary difference being in the parental origin of deletion. Our current understanding of the cytogenetics and molecular genetics of these