22q11 DS: Genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome

International Journal of Developmental Neuroscience

Volumn 20, Issue 3-5, 2002, Pages 407-419

  Maynard, Thomas M ^a   Haskell, Gloria T ^a   Lieberman, Jeffrey A ^a   LaMantia, Anthony Samuel ^a  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

22q11 DS; Gene function; Genome

Indexed keywords

CELL ADHESION MOLECULE; ENZYME;

CELL CYCLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CONGENITAL MALFORMATION; DEPRESSION; DIGEORGE SYNDROME; FACE; GENE DELETION; GENE FUNCTION; HEART; HUMAN; LIMB; MENTAL DISEASE; PRIORITY JOURNAL; REVIEW; SCHIZOPHRENIA; VELOCARDIOFACIAL SYNDROME; ANIMAL; CENTRAL NERVOUS SYSTEM; CHILD; CHROMOSOME 22; CHROMOSOME MAP; DEVELOPMENTAL DISORDER; GENE EXPRESSION REGULATION; GENETICS; GENOME; GROWTH, DEVELOPMENT AND AGING; MAJOR DEPRESSION; METABOLISM; MUTATION; PATHOPHYSIOLOGY; PRENATAL DEVELOPMENT;

ANIMALS; CENTRAL NERVOUS SYSTEM; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 22; DEPRESSIVE DISORDER, MAJOR; DEVELOPMENTAL DISABILITIES; DIGEORGE SYNDROME; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENOME; HUMANS; MUTATION; SCHIZOPHRENIA;

EID: 0035986905     PISSN: 07365748     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0736-5748(02)00050-3     Document Type: Article

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