Impact of genotype-first diagnosis: The detection of microdeletion and microduplication syndromes with cancer predisposition by aCGH

Genetics in Medicine

Volumn 11, Issue 5, 2009, Pages 314-322

  Adams, Sara Anne ^a   Coppinger, Justine ^a   Saitta, Sulagna C ^b   Stroud, Tracy ^c   Kandamurugu, Manikum ^d   Fan, Zheng ^d   Ballif, Blake C ^a   Shaffer, Lisa G ^a,e   Bejjani, Bassem A ^a,e,f  

^a Signature Genomic Laboratories LLC   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^c University of Missouri   (United States)

^d UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^e WASHINGTON STATE UNIVERSITY   (United States)

^f SACRED HEART MEDICAL CENTER   (United States)

Author keywords

Array CGH; Cancer; Comparative genomic hybridization; Mental retardation; Predisposition testing

Indexed keywords

ARTICLE; CANCER GENETICS; CANCER RISK; CANCER SUSCEPTIBILITY; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL MALFORMATION; DEVELOPMENTAL DISORDER; GENE DELETION; GENE DUPLICATION; GENETIC COUNSELING; GENETIC RISK; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MICROARRAY ANALYSIS; PHENOTYPE;

CHILD, PRESCHOOL; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL ABNORMALITIES; DEVELOPMENTAL DISABILITIES; GENE DUPLICATION; GENETIC PREDISPOSITION TO DISEASE; HUMANS; KARYOTYPING; MICROARRAY ANALYSIS; NEOPLASMS; SEQUENCE DELETION;

EID: 67249148525     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/GIM.0b013e3181a028a5     Document Type: Article

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