22q11.2 Deletion Syndrome: Introduction

Child Neuropsychology

Volumn 11, Issue 1, 2005, Pages 1-3

  Lajiness O'Neill, Renée ^a  

^a HENRY FORD HEALTH SYSTEM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID; CATECHOL METHYLTRANSFERASE; PROLINE DEHYDROGENASE; PROLINE DEHYDROGENASE 2; UNCLASSIFIED DRUG;

ADULT; AUTISM; BIPOLAR DISORDER; CHROMOSOME 22Q; CHROMOSOME 22Q11.2 DELETION SYNDROME; CHROMOSOME DELETION; CLINICAL FEATURE; COGNITION; DIGEORGE SYNDROME; EDITORIAL; ENVIRONMENTAL FACTOR; GABRB3 GENE; GENE; GENE DISRUPTION; GENETIC HETEROGENEITY; GENETIC SUSCEPTIBILITY; GENETIC TRAIT; GENETIC VARIABILITY; GENOME IMPRINTING; GENOTYPE PHENOTYPE CORRELATION; HAPPY PUPPET SYNDROME; HUMAN; INTELLIGENCE QUOTIENT; LEARNING; LEARNING DISORDER; MEMORY; NEUROIMAGING; NEUROPSYCHOLOGY; OBSESSIVE COMPULSIVE DISORDER; PENETRANCE; PHENOTYPE; PRADER WILLI SYNDROME; PREFRONTAL CORTEX; SCHIZOPHRENIA; SYMPTOMATOLOGY; VELOCARDIOFACIAL SYNDROME; VERBAL BEHAVIOR;

CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 22; COGNITION DISORDERS; DIGEORGE SYNDROME; HUMANS; NEUROPSYCHOLOGICAL TESTS; PHENOTYPE; POINT MUTATION;

EID: 17144372991     PISSN: 09297049     EISSN: None     Source Type: Journal    
DOI: 10.1080/09297040590911176     Document Type: Editorial

References (7)

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