No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence

British Journal of Haematology

Volumn 109, Issue 1, 2000, Pages 117-120

  Stanulla, Martin ^a   Stümm, Markus ^b   Dieckvoss, Björn Ole ^a   Seidemann, Kathrin ^a   Schemmel, Verena ^a   Brechlin, Annette Müller ^a   Schrappe, Martin ^a   Welte, Karl ^a   Reiter, Alfred ^a,c  

^a HANNOVER MEDICAL SCHOOL   (Germany)

^b OTTO VON GUERICKE UNIVERSITY   (Germany)

^c UNIVERSITY HOSPITAL GIESSEN   (Germany)

Author keywords

Adolescence; Childhood; NBS1; Nijmegen breakage syndrome; Non Hodgkin's lymphoma

Indexed keywords

ADOLESCENT; ARTICLE; CANCER SUSCEPTIBILITY; CARCINOGENESIS; CHILD; DNA DETERMINATION; FEMALE; GENE DELETION; GENE MUTATION; HETEROZYGOTE DETECTION; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; NONHODGKIN LYMPHOMA; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; CELL CYCLE PROTEINS; CHILD; CHILD, PRESCHOOL; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 7; CHROMOSOMES, HUMAN, PAIR 8; DNA MUTATIONAL ANALYSIS; FEMALE; GENE DELETION; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HUMANS; LYMPHOMA, NON-HODGKIN; MALE; NUCLEAR PROTEINS;

EID: 0034085362     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2000.01973.x     Document Type: Article

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