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Angelman syndrome and severe infections in a patient with de novo 15q11.2–q13.1 deletion and maternally inherited 2q21.3 microdeletion

✍ Scribed by Gerda Neubert; Katja von Au; Katrin Drossel; Andreas Tzschach; Denise Horn; Renate Nickel; Angela M. Kaindl

Book ID: 119241505
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 366 KB
Volume: 512
Category: Article
ISSN: 0378-1119
DOI: 10.1016/j.gene.2012.10.061

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