Recurrent 10q22-q23 deletions: A genomic disorder on 10q associated with cognitive and behavioral abnormalities

American Journal of Human Genetics

Volumn 80, Issue 5, 2007, Pages 938-947

  Balciuniene, Jorune ^a,b   Feng, Ningping ^d   Iyadurai, Kelly ^a,b,g   Hirsch, Betsy ^a,b,c   Charnas, Lawrence ^a,b   Bill, Brent R ^a   Easterday, Mathew C ^a,b   Staaf, Johan ^f   Oseth, LeAnn ^a,c   Czapansky Beilman, Desiree ^b   Avramopoulos, Dimitri ^d   Thomas, George H ^d,e   Borg, Åke ^f   Valle, David ^d   Schimmenti, Lisa A ^a,b   Selleck, Scott B ^a,b  

^a UNIVERSITY OF MINNESOTA   (United States)

^b UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^c UNIVERSITY OF MINNESOTA   (United States)

^d JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e KENNEDY KRIEGER INSTITUTE   (United States)

^f LUND UNIVERSITY HOSPITAL   (Sweden)

^g TRANSLATIONAL GENOMICS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA FRAGMENT; REPETITIVE DNA;

ARTICLE; BEHAVIOR DISORDER; CHILD; CHROMOSOMAL INSTABILITY; CHROMOSOME 10Q; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME MAP; CHROMOSOME REARRANGEMENT; COGNITIVE DEFECT; COMPARATIVE GENOMIC HYBRIDIZATION; DELETION MUTANT; FEMALE; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC LINKAGE; HUMAN; MALE; MICROARRAY ANALYSIS; NUCLEOTIDE REPEAT; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

EID: 34247569809     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/513607     Document Type: Article

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