Nijmegen breakage syndrome

Show simple item record Uhrhammer, N fr_FR Bay, JO fr_FR Gatti, RA fr_FR 2011-02-22T15:25:35Z 2011-02-22T15:25:35Z 2003 fr_FR
dc.identifier.citation Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2003, Vol. 7, N° 1 ; p. 57-58 fr_FR
dc.identifier.issn 1768-3262 fr_FR
dc.description Review on Nijmegen breakage syndrome, with data on clinics, and the genes involved. en
dc.language.iso en fr_FR
dc.publisher Jean-Loup Huret (Editor-in-Chief) ; INIST-CNRS (Publisher) fr_FR
dc.relation Atlas of Genetics and Cytogenetics in Oncology and Haematology ; fr_FR
dc.relation.ispartofseries Atlas of Genetics and Cytogenetics in Oncology and Haematology
dc.rights Open access resource - terms and conditions : fr_FR
dc.subject Chromosome 8 fr_FR
dc.subject ataxia-telangiectasia, variant VI (alias) fr_FR
dc.subject Seemanova syndrome II (alias) fr_FR
dc.subject microcephaly with normal intelligence, immunodeficiency, lymphoreticular malignancies (alias) fr_FR
dc.subject immunodeficiency, microcephaly, chromosomal instability (alias) fr_FR
dc.subject.classification Cancer Prone Diseases Section fr_FR
dc.subject.mesh NBN protein, human fr_FR
dc.subject.mesh DNA Repair-Deficiency Disorders fr_FR
dc.subject.mesh Nijmegen Breakage Syndrome fr_FR
dc.title Nijmegen breakage syndrome fr_FR
dc.type Mini Review fr_FR
dc.contributor.affiliation Centre Jean-Perrin, BP 392, 63000 Clermont-Ferrand, France fr_FR

Files in this item

PDF 10-2002-NijmegenID10020.pdf 24.87Kb

This item appears in the following Collection(s)

Show simple item record

Advanced Search