Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities

American Journal of Human Genetics

Volumn 73, Issue 6, 2003, Pages 1261-1270

  Vissers, Lisenka E L M ^a   De Vries, Bert B A ^a   Osoegawa, Kazutoyo ^b   Janssen, Irene M ^a   Feuth, Ton ^a   Choy, Chik On ^b   Straatman, Huub ^a   Van Der Vliet, Walter ^a   Huys, Erik H L P G ^a   Van Rijk, Anke ^a   Smeets, Dominique ^a   Van Ravenswaaij Arts, Conny M A ^a   Knoers, Nine V ^a   Van Der Burgt, Ineke ^a   De Jong, Pieter J ^b   Brunner, Han G ^a   Van Kessel, Ad Geurts ^a   Schoenmakers, Eric F P M ^a   Veltman, Joris A ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b CHILDREN S HOSPITAL OAKLAND RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; CLINICAL ARTICLE; CLONE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; CYTOGENETICS; DIAGNOSTIC ACCURACY; DNA MICROARRAY; DYE SWAP REPLICATE ANALYSIS; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE REPLICATION; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENETIC SCREENING; GENOME; HUMAN; HUMAN CELL; HYBRIDIZATION; MALE; MENTAL DEFICIENCY; MENTAL RETARDATION MALFORMATION SYNDROME; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; SYNDROME DELINEATION; TECHNOLOGY; VALIDATION PROCESS;

EID: 9144240478     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/379977     Document Type: Article

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