Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias

Cancer Research

Volumn 65, Issue 20, 2005, Pages 9152-9154

  Fitzgibbon, Jude ^a   Smith, Lan Lan ^a   Raghavan, Manoj ^a   Smith, Matthew L ^a   Debernardi, Silvana ^a   Skoulakis, Spyros ^a   Lillington, Debra ^a   Lister, T Andrew ^a   Young, Bryan D ^a  

^a IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FLT3 LIGAND; TRANSCRIPTION FACTOR RUNX1; WT1 PROTEIN;

ACUTE GRANULOCYTIC LEUKEMIA; ALLELE; ARTICLE; CYTOGENETICS; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC RECOMBINATION; GENOME ANALYSIS; HOMOZYGOSITY; HUMAN; HUMAN CELL; JAK2 GENE; MUTATIONAL ANALYSIS; MYELOPROLIFERATIVE DISORDER; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; UNIPARENTAL DISOMY; WILD TYPE;

ACUTE DISEASE; BASE SEQUENCE; CCAAT-ENHANCER-BINDING PROTEIN-ALPHA; CORE BINDING FACTOR ALPHA 2 SUBUNIT; FMS-LIKE TYROSINE KINASE 3; GENES, WILMS TUMOR; HUMANS; LEUKEMIA, MYELOID; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; UNIPARENTAL DISOMY;

EID: 27144478643     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: 10.1158/0008-5472.CAN-05-2017     Document Type: Article

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