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Volumn 159, Issue 4, 2002, Pages 527-
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The human genome: Chromosome 22q11 deletion syndrome
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Author keywords
[No Author keywords available]
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Indexed keywords
DNA;
RNA;
ARTICLE;
CASE REPORT;
CHROMOSOME 22Q;
CHROMOSOME DELETION;
CHROMOSOME REARRANGEMENT;
CYTOGENETICS;
DEVELOPMENTAL DISORDER;
DIGEORGE SYNDROME;
DISEASE SEVERITY;
DNA PROBE;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENE DELETION;
HUMAN;
HUMAN GENOME;
INCIDENCE;
LEARNING DISORDER;
MANIC DEPRESSIVE PSYCHOSIS;
METAPHASE;
NEUROPSYCHIATRY;
PHENOTYPE;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
RNA PROBE;
SCHIZOPHRENIA;
STRUCTURAL CHROMOSOME ABERRATION;
VELOCARDIOFACIAL SYNDROME;
CHILD, PRESCHOOL;
CHROMOSOME DELETION;
CHROMOSOMES, HUMAN, PAIR 22;
DIGEORGE SYNDROME;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
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EID: 0036218548
PISSN: 0002953X
EISSN: None
Source Type: Journal
DOI: 10.1176/appi.ajp.159.4.527 Document Type: Article |
Times cited : (2)
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References (0)
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