Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders

American Journal of Human Genetics

Volumn 95, Issue 4, 2014, Pages 454-461

  Brand, Harrison ^a   Pillalamarri, Vamsee ^a   Collins, Ryan L ^a,b   Eggert, Stacey ^c   O'Dushlaine, Colm ^a   Braaten, Ellen B ^a   Stone, Matthew R ^a   Chambert, Kimberly ^c   Doty, Nathan D ^a   Hanscom, Carrie ^a   Rosenfeld, Jill A ^d,g   Ditmars, Hillary ^a   Blais, Jessica ^a   Mills, Ryan ^e   Lee, Charles ^f   Gusella, James F ^a,b,c   McCarroll, Steven ^b,c   Smoller, Jordan W ^a,c   Talkowski, Michael E ^a,c   Doyle, Alysa E ^a,c  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^d PERKINELMER INC   (United States)

^e UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

^f JACKSON LABORATORY   (United States)

^g BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; BIPOLAR DISORDER; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CHROMOSOME REARRANGEMENT; CLASSIFICATION ALGORITHM; COMPLEX CHROMOSOMAL ABERRATION; CRYPTIC CHROMOSOMAL ABERRATION; CYTOGENETICS; GAIN OF FUNCTION MUTATION; GENE EXPRESSION PROFILING; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC VARIABILITY; GILLES DE LA TOURETTE SYNDROME; HAPLOINSUFFICIENCY; HUMAN; INTELLECTUAL IMPAIRMENT; LOSS OF FUNCTION MUTATION; MENTAL DISEASE; NEUROLOGIC DISEASE; PRIORITY JOURNAL; PSYCHOSIS; SCHIZOPHRENIA; SEGMENTAL DUPLICATION; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; GENETICS; HUMAN CHROMOSOME; HUMAN GENOME; MENTAL DISORDERS; MICROARRAY ANALYSIS; NEURODEGENERATIVE DISEASES; ONSET AGE; PHENOTYPE; UNITED STATES;

AGE OF ONSET; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN; COMPARATIVE GENOMIC HYBRIDIZATION; DNA COPY NUMBER VARIATIONS; GENOME, HUMAN; HUMANS; MENTAL DISORDERS; MICROARRAY ANALYSIS; NEURODEGENERATIVE DISEASES; PHENOTYPE; UNITED STATES;

EID: 84921718161     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2014.09.005     Document Type: Article

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