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W01-02 - Neuropsychiatric aspects of the 22q11 microdeletion syndrome

✍ Scribed by Gawlik, M.; Pfuhlmann, B.; Stöber, G.


Book ID
122822021
Publisher
Elsevier Science
Year
2012
Tongue
French
Weight
92 KB
Volume
27
Category
Article
ISSN
0924-9338

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## Communicated by Riccardo Fodde The 22q11.2 microdeletion syndrome is the most frequent microdeletion syndrome in humans, yet its genetic basis is complex and is still not fully understood. Most patients harbor a 3-Mb deletion (typically deleted region [TDR]), but occasionally patients with atypi