High prevalence of theNBN gene mutation c.657-661del5 in Southeast Germany
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF03195730.pdf
Reference25 articles.
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3. Carlomagno F, Chang-Claude J, Dunning AM, Ponder BA, 1999. Determination of the frequency of the common 657Del5 Nijmegen breakage syndrome mutation in the German population: no association with risk of breast cancer. Genes Chromosomes Cancer 25: 393–395.
4. Carney JP, Maser RS, Olivares H, Davis EM, LeBeau M, Yates JR 3rd, et al. 1998. The hMre1 1/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response. Cell 93: 477–486.
5. Chrzanowska KH, Kleijer WJ, Krajewska-Walasek M, Białecka M, Gutkowska A, Goryluk-Kozakiewicz B, et al. 1995. Eleven Polish patients with microcephaly, immunodeficiency, and chromosomal instability: the Nijmegen breakage syndrome. Am J Med Genet 57: 462–471.
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