Genomic variation by whole-genome SNP mapping arrays predicts time-to-event outcome in patients with chronic lymphocytic Leukemia: A comparison of CLL and HapMap genotypes

Journal of Molecular Diagnostics

Volumn 15, Issue 2, 2013, Pages 196-209

  Schweighofer, Carmen D ^a   Coombes, Kevin R ^a   Majewski, Tadeusz ^a   Barron, Lynn L ^a   Lerner, Susan ^a   Sargent, Rachel L ^a   O'Brien, Susan ^a   Ferrajoli, Alessandra ^a   Wierda, William G ^a   Czerniak, Bogdan A ^a   Medeiros, L Jeffrey ^a   Keating, Michael J ^a   Abruzzo, Lynne V ^a  

^a UNIVERSITY OF TEXAS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ANALYTIC METHOD; ARTICLE; CANCER PATIENT; CANCER SURVIVAL; CHROMOSOME 11P; CHROMOSOME 11Q; CHROMOSOME 17P; CHROMOSOME 2P; CHROMOSOME 4P; CHROMOSOME 4Q; CHROMOSOME 6P; CHROMOSOME 6Q; CHROMOSOME 7Q; CHROMOSOME DELETION; CHRONIC LYMPHATIC LEUKEMIA; CONTROLLED STUDY; COPY NUMBER VARIATION; FEMALE; GENETIC VARIABILITY; GENOTYPE; HUMAN; HUMAN CELL; MALE; OUTCOME ASSESSMENT; OVERALL SURVIVAL; SINGLE NUCLEOTIDE POLYMORPHISM; TIME TO TREATMENT;

ADULT; AGED; CHROMOSOME ABERRATIONS; DNA COPY NUMBER VARIATIONS; FEMALE; FOLLOW-UP STUDIES; GENOME, HUMAN; GENOMICS; GENOTYPE; HUMANS; LEUKEMIA, LYMPHOCYTIC, CHRONIC, B-CELL; MALE; MIDDLE AGED; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; PROGNOSIS;

EID: 84874548075     PISSN: 15251578     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jmoldx.2012.09.006     Document Type: Article

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