Identification of a novel deletion region in 3q29 microdeletion syndrome by oligonucleotide array comparative genomic hybridization

Korean Journal of Laboratory Medicine

Volumn 30, Issue 1, 2010, Pages 70-75

  Seo, Eul Ju ^a   Jun, Kyung Ran ^a   Yoo, Han Wook ^a   Yoo, Hanik K ^a   Lee, Jin Ok ^b  

^a University of Ulsan College of Medicine   (South Korea)

^b Asan Institute for Life Sciences   (South Korea)

Author keywords

Chromosome deletion; Chromosome disorders; Comparative genomic hybridization; Human chromosome pair 3; Microarray analysis

Indexed keywords

BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; DLG1 PROTEIN, HUMAN; HES1 PROTEIN, HUMAN; HOMEODOMAIN PROTEIN; MELANOMA ANTIGEN; MEMBRANE PROTEIN; P21 ACTIVATED KINASE; PAK2 PROTEIN, HUMAN; SIGNAL TRANSDUCING ADAPTOR PROTEIN;

ADOLESCENT; ARTICLE; ATTENTION DEFICIT DISORDER; CASE REPORT; CHROMOSOME 3; CHROMOSOME DELETION; CHROMOSOME DISORDER; COMPARATIVE GENOMIC HYBRIDIZATION; DNA MICROARRAY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; METHODOLOGY; SYNDROME; TWINS;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ADOLESCENT; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 3; COMPARATIVE GENOMIC HYBRIDIZATION; DISEASES IN TWINS; FEMALE; HOMEODOMAIN PROTEINS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MELANOMA-SPECIFIC ANTIGENS; MEMBRANE PROTEINS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; P21-ACTIVATED KINASES; SYNDROME; TWINS;

EID: 77954853276     PISSN: 15986535     EISSN: None     Source Type: Journal    
DOI: 10.3343/kjlm.2010.30.1.70     Document Type: Article

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