Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: A preliminary study

Archives of General Psychiatry

Volumn 58, Issue 1, 2001, Pages 64-68

  Eliez, Stephan ^a   Antonarakis, Stylianos E ^b   Morris, Michael A ^b   Dahoun, Sophie P ^b   Reiss, Allan L ^a  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF GENEVA   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; BRAIN DEVELOPMENT; BRAIN SIZE; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CONGENITAL HEART MALFORMATION; DISEASE PREDISPOSITION; DNA POLYMORPHISM; FEMALE; GRAY MATTER; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; SCHIZOPHRENIA; VELOCARDIOFACIAL SYNDROME; WHITE MATTER;

EID: 0035176185     PISSN: 0003990X     EISSN: None     Source Type: Journal    
DOI: 10.1001/archpsyc.58.1.64     Document Type: Article

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