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Volumn 25, Issue 11, 2011, Pages 1782-1784
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Rare germline variants in regions of loss of heterozygosity may influence clinical course of hematological malignancies
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Author keywords
[No Author keywords available]
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Indexed keywords
CBL PROTEIN;
ERYTHROPOIETIN;
GENOMIC DNA;
JANUS KINASE 2;
TRANSCRIPTION FACTOR EZH2;
ACUTE GRANULOCYTIC LEUKEMIA;
ALLELE;
BLOOD;
BLOOD TRANSFUSION;
CHEEK MUCOSA;
CHROMOSOME 14Q;
CHROMOSOME 9P;
CHROMOSOME ARM;
DAUGHTER CELL;
EXOME;
EXON;
FANCONI ANEMIA;
GENE SEQUENCE;
GRANULOCYTE;
HEMATOCRIT;
HETEROZYGOSITY;
HUMAN;
HUMAN GENOME PROJECT;
KARYOTYPING;
LETTER;
LEUKOCYTE COUNT;
LEUKOCYTOSIS;
NONSENSE MUTATION;
PEDIGREE ANALYSIS;
PHENOTYPE;
PHLEBOTOMY;
POLYCYTHEMIA VERA;
PRIORITY JOURNAL;
SINGLE NUCLEOTIDE POLYMORPHISM;
SOMATIC MUTATION;
TELOMERE;
THROMBOCYTOSIS;
UNIPARENTAL DISOMY;
GERM-LINE MUTATION;
HEMATOLOGIC NEOPLASMS;
HUMANS;
LOSS OF HETEROZYGOSITY;
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EID: 80755132100
PISSN: 08876924
EISSN: 14765551
Source Type: Journal
DOI: 10.1038/leu.2011.150 Document Type: Letter |
Times cited : (6)
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References (6)
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