Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias

Cancer Research

Volumn 65, Issue 2, 2005, Pages 375-378

  Raghavan, Manoj ^a   Lillington, Debra M ^a   Skoulakis, Spyros ^a   Debernardi, Silvana ^a   Chaplin, Tracy ^a   Foot, Nicola J ^a   Lister, T Andrew ^a   Young, Bryan D ^a,b  

^a QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^b IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ARTICLE; BONE MARROW; CANCER GENETICS; CELL CLONE; CHROMOSOME 19; CHROMOSOME ABERRATION; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENOME ANALYSIS; HOMOZYGOSITY; HUMAN; KARYOTYPE; METHYLATION; MICROSATELLITE MARKER; MITOTIC RECOMBINATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; REMISSION; SINGLE NUCLEOTIDE POLYMORPHISM; UNIPARENTAL DISOMY;

ACUTE DISEASE; ADULT; AGED; AGED, 80 AND OVER; BASE SEQUENCE; DIPLOIDY; DNA METHYLATION; DNA, NEOPLASM; FEMALE; GENOME, HUMAN; HUMANS; KARYOTYPING; LEUKEMIA, MYELOID; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; UNIPARENTAL DISOMY;

EID: 12544257171     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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