Cytogenetic Abnormalities in Attention-Deficit/Hyperactivity Disorder

Journal of the American Academy of Child and Adolescent Psychiatry

Volumn 41, Issue 7, 2002, Pages 806-810

  Bastain, Theresa M ^a   Lewczyk, Caroline M ^a   Sharp, Wendy S ^a   James, Regina S ^a   Long, Robert T ^a   Eagen, Patricia B ^a   Ebens, Christen L ^a   Meck, Jeanne M ^a   Chan, Wai Yee ^a   Sidransky, Ellen ^a   Rapoport, Judith L ^a   Castellanos, F Xavier ^a,b  

^a GEORGETOWN UNIVERSITY MEDICAL CENTER   (United States)

^b NEW YORK UNIVERSITY CHILD STUDY CENTER   (United States)

Author keywords

Attention deficit hyperactivity disorder; Cytogenetics; Fragile X; Velocardiofacial syndrome

Indexed keywords

ADOLESCENT; ANEUPLOIDY; ARTICLE; ATTENTION DEFICIT DISORDER; CHROMOSOME 22Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; CONTROLLED STUDY; FAMILY HISTORY; FEMALE; FRAGILE X SYNDROME; GENE MUTATION; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SCHOOL CHILD; VELOCARDIOFACIAL SYNDROME; X CHROMOSOME; CHILD; CHROMOSOME 22; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; CYTOGENETICS; FACE; GENETICS; METHODOLOGY; MULTIPLE MALFORMATION SYNDROME; SOFT PALATE; SYNDROME;

ABNORMALITIES, MULTIPLE; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; CHILD; CHROMOSOMES, HUMAN, PAIR 22; CYTOGENETICS; FACE; FEMALE; FRAGILE X SYNDROME; HEART DEFECTS, CONGENITAL; HUMANS; MALE; PALATE, SOFT; SYNDROME;

EID: 0036631863     PISSN: 08908567     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004583-200207000-00012     Document Type: Article

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