Congenital heart disease affects local gyrification in 22q11.2 deletion syndrome

Developmental Medicine and Child Neurology

Volumn 51, Issue 9, 2009, Pages 746-753

  Schaer, Marie ^a,b   Glaser, Bronwyn ^a   Cuadra, Meritxell Bach ^b   Debbane, Martin ^a   Thiran, Jean Philippe ^b   Eliez, Stephan ^a  

^a UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

^b EPFL   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BRAIN CORTEX; BRAIN DEVELOPMENT; BRAIN INJURY; CELL MIGRATION; CELL PROLIFERATION; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CHROMOSOME DISORDER; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; CONTROLLED STUDY; GYRUS; HEMODYNAMICS; HUMAN; MICROGYRIA; NERVE CELL; NERVE CELL DIFFERENTIATION; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; THREE DIMENSIONAL IMAGING;

ADOLESCENT; ADULT; CASE-CONTROL STUDIES; CEREBRAL CORTEX; CHILD; COHORT STUDIES; DIGEORGE SYNDROME; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; IMAGING, THREE-DIMENSIONAL; MAGNETIC RESONANCE IMAGING; MALE; ORGAN SIZE; YOUNG ADULT;

EID: 67651092561     PISSN: 00121622     EISSN: 14698749     Source Type: Journal    
DOI: 10.1111/j.1469-8749.2009.03281.x     Document Type: Article

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