Literature DB >> 14559852

Correspondence re: R. Varon et al., Mutations in the Nijmegen breakage syndrome gene (NBS1) in childhood acute lymphoblastic leukemia. Cancer Res., 61: 3570-3572, 2001.

G Malcolm Taylor, Helen P O'Brien, Melvyn F Greaves, Paul F Ravetto, Osborn B Eden.   

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Year:  2003        PMID： 14559852

Source DB:  PubMed          Journal:  Cancer Res        ISSN： 0008-5472            Impact factor:   12.701


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  5 in total

1.  High prevalence of the NBN gene mutation c.657-661del5 in Southeast Germany.

Authors:  M H Maurer; K Hoffmann; K Sperling; R Varon
Journal:  J Appl Genet       Date:  2010       Impact factor: 3.240

Review 2.  Ataxia-telangiectasia and related diseases.

Authors:  Pierre-Olivier Frappart; Peter J McKinnon
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

3.  Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability.

Authors:  E Seemanová; K Sperling; H Neitzel; R Varon; J Hadac; O Butova; E Schröck; P Seeman; M Digweed
Journal:  J Med Genet       Date:  2005-07-20       Impact factor: 6.318

4.  NBN Gene Polymorphisms and Cancer Susceptibility: A Systemic Review.

Authors:  Francesco Berardinelli; Alessandra di Masi; Antonio Antoccia
Journal:  Curr Genomics       Date:  2013-11       Impact factor: 2.236

5.  NBS1 Heterozygosity and Cancer Risk.

Authors:  Alessandra di Masi; Antonio Antoccia
Journal:  Curr Genomics       Date:  2008-06       Impact factor: 2.236
  5 in total

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