Mutation analysis of the Nijmegen Breakage Syndrome gene (NBS1) in nineteen patients with acute myeloid leukemia with complex karyotypes

Leukemia and Lymphoma

Volumn 44, Issue 11, 2003, Pages 1931-1934

  Varon, Raymonda ^a   Schoch, Claudia ^b   Reis, André ^d   Hiddemann, Wolfgang ^b,c   Sperling, Karl ^a   Schnittger, Susanne ^b  

^a HUMBOLDT UNIVERSITY   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

^c INSTITUTE OF EPIDEMIOLOGY   (Germany)

^d UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

AML; Complex karyotype; Mutation analysis; NBSI gene

Indexed keywords

DOUBLE STRANDED DNA; GENE PRODUCT;

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; AGED; AMPLICON; ARTICLE; BINDING SITE; CANCER SUSCEPTIBILITY; CHROMOSOME ABERRATION; CHROMOSOME DISORDER; CLINICAL ARTICLE; CONTROLLED STUDY; DNA DETERMINATION; DNA STRAND BREAKAGE; EXON; FEMALE; GENE DELETION; GENE MUTATION; GENE SEQUENCE; GENETIC POLYMORPHISM; GENETIC STABILITY; HETEROZYGOSITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; IMMUNE DEFICIENCY; INTRON; IONIZING RADIATION; KARYOTYPE; LEUKEMOGENESIS; MALE; MUTATIONAL ANALYSIS; NIJMEGEN BREAKAGE SYNDROME; PRIORITY JOURNAL; RADIOSENSITIVITY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA SPLICING; SAMPLE;

ACUTE DISEASE; ADULT; AGED; CELL CYCLE PROTEINS; DNA MUTATIONAL ANALYSIS; DNA, NEOPLASM; EXONS; FEMALE; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; INTRONS; KARYOTYPING; LEUKEMIA, MYELOID; MALE; MIDDLE AGED; MUTATION; NUCLEAR PROTEINS; SEQUENCE DELETION; SYNDROME;

EID: 0242635676     PISSN: 10428194     EISSN: None     Source Type: Journal    
DOI: 10.1080/1042819031000099724     Document Type: Article

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