Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)

Neurogenetics

Volumn 10, Issue 2, 2009, Pages 89-95

  Coldren, C D ^a   Lai, Z ^b   Shragg, P ^c   Rossi, E ^d   Glidewell, S C ^a   Zuffardi, O ^d   Mattina, T ^e   Ivy, D D ^f   Curfs, L M ^g   Mattson, S N ^h   Riley, E P ^h   Treier, M ⁱ   Grossfeld, P D ^j,k  

^a UNIVERSITY OF COLORADO   (United States)

^b UCSD School of Medicine ^*

^c UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^d UNIVERSITY OF PAVIA   (Italy)

^e UNIVERSITY OF CATANIA   (Italy)

^f CHILDREN S HOSPITAL   (United States)

^g MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^h SAN DIEGO STATE UNIVERSITY   (United States)

ⁱ EUROPEAN MOLECULAR BIOLOGY LABORATORY   (Germany)

^j UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^k Division of Pediatric Cardiology   (United Kingdom)

more..

Author keywords

Brain specific homeobox protein; Cognition; Comparative genomic hybridization; Jacobsen syndrome; Neurogranin

Indexed keywords

BRAIN SPECIFIC HOMEOBOX PROTEIN BSX; HOMEODOMAIN PROTEIN; NEUROGRANIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; ATTENTION; AUDITORY ATTENTION; BEHAVIOR DISORDER; BSX GENE; CHILD; CHROMOSOME 11Q; CHROMOSOME DELETION; CHROMOSOME MAP; CLINICAL ARTICLE; COGNITIVE DEFECT; DISEASE SEVERITY; DISTRACTIBILITY; FEMALE; GENE; GENE LOCUS; HUMAN; INTELLIGENCE QUOTIENT; JACOBSEN SYNDROME; MALE; MICROARRAY ANALYSIS; NEUROGRANIN GENE; NEUROPSYCHOLOGICAL TEST; PRIORITY JOURNAL;

MUS;

EID: 64149094521     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10048-008-0157-x     Document Type: Article

References (13)

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