Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia

American Journal of Human Genetics

Volumn 87, Issue 5, 2010, Pages 618-630

  Moreno De Luca, Daniel ^a   Mulle, Jennifer G ^a   Kaminsky, Erin B ^a   Sanders, Stephan J ^b   Myers, Scott M ^c   Adam, Margaret P ^a   Pakula, Amy T ^a   Eisenhauer, Nancy J ^c   Uhas, Kim ^a   Weik, Luann ^d   Guy, Lisa ^a   Care, Melanie E ^e   Morel, Chantal F ^e   Boni, Charlotte ^c   Salbert, Bonnie Anne ^c   Chandrareddy, Ashadeep ^f   Demmer, Laurie A ^f   Chow, Eva W C ^g   Surti, Urvashi ^h   Aradhya, Swaroop ⁱ   Pickering, Diane L ^j   Golden, Denae M ^j   Sanger, Warren G ^j   Aston, Emily ^k   Brothman, Arthur R ^k   Gliem, Troy J ^l   Thorland, Erik C ^l   Ackley, Todd ^m   Iyer, Ram ^m   Huang, Shuwen ⁿ   Barber, John C ⁿ   Crolla, John A ⁿ   Warren, Stephen T ^a   Martin, Christa L ^a   Ledbetter, David H ^a   more..

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c GEISINGER MEDICAL CENTER   (United States)

^d CHILDREN S HOSPITAL OF WISCONSIN   (United States)

^e UNIVERSITY HEALTH NETWORK   (Canada)

^f TUFTS MEDICAL CENTER   (United States)

^g UNIVERSITY OF TORONTO   (Canada)

^h UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

ⁱ GENEDX   (United States)

^j UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

^k ARUP LABORATORIES   (United States)

^l MAYO CLINIC   (United States)

^m Michigan Medical Genetics Laboratories   (United States)

ⁿ SALISBURY NHS FOUNDATION TRUST   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTISM; CHILD; CHROMOSOME DELETION; CHROMOSOME DELETION 17Q12; CLINICAL ARTICLE; COGNITIVE DEFECT; CONTROLLED STUDY; COPY NUMBER VARIATION; FACIES; FEMALE; FOLLOW UP; GENE; GENETIC RISK; HNF1B GENE; HUMAN; KIDNEY MALFORMATION; MACROCEPHALY; MALE; PHENOTYPE; PRIORITY JOURNAL; RISK FACTOR; SCHIZOPHRENIA;

CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 17; DNA COPY NUMBER VARIATIONS; FACIES; FEMALE; HUMANS; MALE; PHENOTYPE; SCHIZOPHRENIA; SEQUENCE DELETION;

EID: 78249281977     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajhg.2010.10.004     Document Type: Article

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