High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs

American Journal of Human Genetics

Volumn 77, Issue 5, 2005, Pages 709-726

  Slater, Howard R ^a,b,c   Bailey, Dione K ^e   Ren, Hua ^c   Cao, Manqiu ^f   Bell, Katrina ^c   Nasioulas, Steven ^a   Henke, Robert ^d   Choo, K H Andy ^b,c   Kennedy, Giulia C ^e  

^a Genetic Health Cytogenetics Laboratory   (Australia)

^b UNIVERSITY OF MELBOURNE   (Australia)

^c ROYAL CHILDREN'S HOSPITAL   (Australia)

^d Millennium Biosciences   (Australia)

^e Thermo Fisher Scientific   (United States)

^f NONE

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ACUTE LYMPHOCYTIC LEUKEMIA; ARTICLE; CHROMATIN; CHROMOSOME 15; CHROMOSOME 17P; CHROMOSOME 6P; CHROMOSOME 7P; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME MAP; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; FAMILY STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; KARYOTYPE; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; TRISOMY;

EID: 27244449351     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/497343     Document Type: Article

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