Genome-wide mapping of copy number variations using SNP arrays

Transfusion Medicine and Hemotherapy

Volumn 36, Issue 4, 2009, Pages 246-251

  Nowak, Daniel ^a   Hofmann, Wolf Karsten ^b   Koeffler, H Phillip ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b Department of Hematology and Oncology   (Germany)

Author keywords

SNP array

Indexed keywords

BCR ABL PROTEIN;

ACUTE LYMPHOBLASTIC LEUKEMIA; CHROMOSOME ANALYSIS; DIAGNOSTIC ACCURACY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE DELETION; GENE MAPPING; GENE MUTATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; HETEROZYGOSITY; HUMAN; ONCOGENE; POINT MUTATION; PROGNOSIS; REAL TIME POLYMERASE CHAIN REACTION; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM; UNIPARENTAL DISOMY;

EID: 69549105984     PISSN: 16603796     EISSN: None     Source Type: Journal    
DOI: 10.1159/000225372     Document Type: Review

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