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

Author:

Neubert Gerda,von Au Katja,Drossel Katrin,Tzschach Andreas,Horn Denise,Nickel Renate,Kaindl Angela M.

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference8 articles.

1. Association between a GABRB3 polymorphism and autism;Buxbaum;Mol. Psychiatry,2002

2. Evidence suggesting the inheritance mode of the human P gene in skin complexion is not strictly recessive;Chiang;Am. J. Med. Genet. A,2008

3. Molecular and clinical aspects of Angelman syndrome;Dagli;Mol. Syndr.,2012

4. Sudden death and Angelman syndrome;Herbst;J. Forensic Sci.,2012

5. Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene;Kayser;Am. J. Hum. Genet.,2008

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