Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions

Human Molecular Genetics

Volumn 12, Issue 17, 2003, Pages 2145-2152

  Yu, Wei ^a   Ballif, Blake C ^a   Kashork, Catherine D ^a   Heilstedt, Heidi A ^a   Howard, Leslie A ^a   Cai, Wei Wen ^a   White, Lisa D ^a   Liu, Wenbin ^a   Beaudet, Arthur L ^a   Bejjani, Bassem A ^b   Shaw, Chad A ^a   Shaffer, Lisa G ^b  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b WASHINGTON STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONTIG; MICROSATELLITE DNA;

ANALYTIC METHOD; ARTICLE; BIRTH DEFECT; CANCER DIAGNOSIS; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; CHROMOSOME SIZE; CHROMOSOME STRUCTURE; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL DISORDER; CONTROLLED STUDY; DIAGNOSTIC PROCEDURE; DNA HYBRIDIZATION; DNA MICROARRAY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE CONSTRUCT; GENE DELETION; GENE DOSAGE; GENE INSERTION; GENE STRUCTURE; GENE TECHNOLOGY; GENETIC ANALYSIS; GENETIC DISORDER; HUMAN; HUMAN CELL; INTERSTITIAL CHROMOSOME DELETION; MENTAL DEFICIENCY; MOLECULAR CLONING; PHENOTYPE; PRIORITY JOURNAL; SENSITIVITY ANALYSIS; STRUCTURAL CHROMOSOME ABERRATION; TELOMERE; X CHROMOSOME; Y CHROMOSOME;

CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 1; GENOME, HUMAN; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MICROSATELLITE REPEATS; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY; TELOMERE;

INSERTION SEQUENCES;

EID: 10744221541     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/ddg230     Document Type: Article

References (29)

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