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
Open Access
- 1 April 2000
- journal article
- research article
- Published by Wiley in British Journal of Haematology
- Vol. 109 (1) , 117-120
- https://doi.org/10.1046/j.1365-2141.2000.01973.x
Abstract
The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.Keywords
This publication has 8 references indexed in Scilit:
- Determination of the frequency of the common 657Del5 Nnijmegen breakage syndrome mutation in the German population: No association with risk of breast cancerGenes, Chromosomes and Cancer, 1999
- Characterization of Seven Low Incidence Blood Group Antigens Carried by Erythrocyte Band 3 ProteinBlood, 1998
- Positional cloning of the gene for Nijmegen breakage syndromeNature Genetics, 1998
- Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage SyndromePublished by Elsevier ,1998
- The hMre11/hRad50 Protein Complex and Nijmegen Breakage Syndrome: Linkage of Double-Strand Break Repair to the Cellular DNA Damage ResponseCell, 1998
- Non-Hodgkin's lymphomas of childhood and adolescence: results of a treatment stratified for biologic subtypes and stage--a report of the Berlin-Frankfurt-Münster Group.Journal of Clinical Oncology, 1995
- Therapiestudie NHL-BFM 90 zur Behandlung maligner Non-Hodgkin-Lymphome bei Kindern und Jugendlichen - Teil 1: Klassifikation und Einteilung in strategische TherapiegruppenKlinische Padiatrie, 1994
- An increased risk for malignant neoplasms in heterozygotes for a syndrome of microcephaly, normal intelligence, growth retardation, remarkable facies, immunodeficiency and chromosomal instabilityMutation Research/Reviews in Genetic Toxicology, 1990