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Volumn 14, Issue 1, 2008, Pages 26-34
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Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome
a
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Author keywords
22q11.2; COMT; GNB1L; PRODH; Schizophrenia; Tbx1; VCFS
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Indexed keywords
CATECHOL METHYLTRANSFERASE;
DNA;
GUANINE NUCLEOTIDE BINDING PROTEIN;
PROLINE DEHYDROGENASE;
PROLINE DERIVATIVE;
TRANSCRIPTION FACTOR T BET;
ALLELE;
ANXIETY;
ANXIETY DISORDER;
ATTENTION DEFICIT DISORDER;
AUTISM;
BEHAVIOR DISORDER;
BEHAVIOR GENETICS;
BIPOLAR DISORDER;
CHROMOSOME 22Q;
CHROMOSOME DELETION;
CLINICAL FEATURE;
COGNITIVE DEFECT;
DEPRESSION;
DIAGNOSTIC AND STATISTICAL MANUAL OF MENTAL DISORDERS;
DNA POLYMORPHISM;
DYSTHYMIA;
ENZYMATIC DEGRADATION;
GENE DELETION;
GENE FUNCTION;
GENE LOCATION;
GENE MAPPING;
GENE MUTATION;
GENE SEQUENCE;
GENETIC CODE;
GENETIC SUSCEPTIBILITY;
GENOTYPE;
HEMIZYGOSITY;
HUMAN;
HYPERPROLINEMIA;
INTELLECTUAL IMPAIRMENT;
LEARNING DISORDER;
MOOD DISORDER;
MULTIGENE FAMILY;
NONHUMAN;
OBSESSIVE COMPULSIVE DISORDER;
PHENOTYPE;
PRIORITY JOURNAL;
PROGNOSIS;
REVIEW;
SCHIZOPHRENIA;
SOCIAL DISABILITY;
SOCIAL PROBLEM;
VELOCARDIOFACIAL SYNDROME;
ZINC FINGER MOTIF;
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EID: 44149113011
PISSN: 19405510
EISSN: None
Source Type: Journal
DOI: 10.1002/ddrr.5 Document Type: Review |
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Times cited : (60)
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References (119)
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