Relative burden of large CNVs on a range of neurodevelopmental phenotypes

PLoS Genetics

Volumn 7, Issue 11, 2011, Pages

  Girirajan, Santhosh ^a   Brkanac, Zoran ^a   Coe, Bradley P ^a   Baker, Carl ^a   Vives, Laura ^a   Vu, Tiffany H ^a   Shafer, Neil ^a   Bernier, Raphael ^a   Ferrero, Giovanni B ^b   Silengo, Margherita ^b   Warren, Stephen T ^c   Moreno, Carlos S ^c   Fichera, Marco ^d   Romano, Corrado ^d   Raskind, Wendy H ^a   Eichler, Evan E ^a  

^a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF TURIN   (Italy)

^c EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d OASI RESEARCH INSTITUTE IRCCS   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; AUTISM; CHILD; CHILDHOOD DISABILITY; COHORT ANALYSIS; CONGENITAL MALFORMATION; CONTROLLED STUDY; COPY NUMBER VARIATION; CORRELATION ANALYSIS; DISABILITY; DISEASE SEVERITY; DYSLEXIA; FEMALE; GENOMICS; HUMAN; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; MALE; MICROARRAY ANALYSIS; NEUROLOGIC DISEASE; PHENOTYPE; PRESCHOOL CHILD; SCHOOL CHILD; COMPARATIVE GENOMIC HYBRIDIZATION; GENE DELETION; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETICS; IMMUNOLOGY; METHODOLOGY; NERVOUS SYSTEM DEVELOPMENT; NERVOUS SYSTEM MALFORMATION; PATHOLOGY;

AUTS2 PROTEIN, HUMAN; FORKHEAD TRANSCRIPTION FACTOR; FOXP1 PROTEIN, HUMAN; IMMP2L PROTEIN, HUMAN; PROTEIN; PROTEINASE; REPRESSOR PROTEIN;

ADOLESCENT; AUTISTIC DISORDER; CHILD; COMPARATIVE GENOMIC HYBRIDIZATION; DNA COPY NUMBER VARIATIONS; DYSLEXIA; ENDOPEPTIDASES; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INTELLECTUAL DISABILITY; MALE; NERVOUS SYSTEM MALFORMATIONS; NEUROGENESIS; PHENOTYPE; PROTEINS; REPRESSOR PROTEINS; SEQUENCE DELETION;

EID: 81755183108     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1002334     Document Type: Article

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