A comprehensive analysis of 22q11 gene expression in the developing and adult brain

Proceedings of the National Academy of Sciences of the United States of America

Volumn 100, Issue SUPPL. 2, 2003, Pages 14433-14438

  Maynard, T M ^a   Haskell, G T ^a   Peters, A Z ^a   Sikich, L ^a   Lieberman, J A ^a   LaMantia, A S ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN DEVELOPMENT; CELL MATURATION; CENTRAL NERVOUS SYSTEM; CHROMOSOME 22Q; CHROMOSOME DELETION; CRANIOFACIAL MALFORMATION; DIGEORGE SYNDROME; EMBRYO; FOREBRAIN; GENE; GENE EXPRESSION; GENETIC ANALYSIS; GENETIC LINKAGE; HEART; INCIDENCE; LEARNING DISORDER; LIMB; MOUSE; NERVE CELL; NERVE CELL NETWORK; NONHUMAN; ORTHOLOGY; PERINATAL PERIOD; PHENOTYPE; PRIORITY JOURNAL; PRODH2 GENE; SCHIZOPHRENIA; T10 GENE; TBX1 GENE; VELOCARDIOFACIAL SYNDROME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; AGED; ANIMALS; BRAIN; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; COGNITION DISORDERS; CRANIOFACIAL ABNORMALITIES; GENE EXPRESSION; GENE EXPRESSION PROFILING; HEART DEFECTS, CONGENITAL; HUMANS; LIMB DEFORMITIES, CONGENITAL; MALE; MICE; MICE, INBRED ICR; MICE, KNOCKOUT; MIDDLE AGED; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; RATS; SCHIZOPHRENIA; SYNDROME;

EID: 0345060815     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.2235651100     Document Type: Article

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