Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Nijmegen Breakage Syndrome and NBN[original query] |
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| Cancer risk of heterozygotes with the NBN founder mutation. Journal of the National Cancer Institute 2007 Dec 99 (24): 1875-80. Seemanová Eva, Jarolim Petr, Seeman Pavel, Varon Raymonda, Digweed Martin, Swift Michael, Sperling Ka |
| Variations in the NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2 French Canadian families with high risk of breast cancer. BMC cancer 2009 9 (1): 181. Desjardins Sylvie, Beauparlant Joly Charles, Labrie Yvan, Ouellette Geneviève, Durocher Francine, |
| NBN 657del5 heterozygous mutations and colorectal cancer risk in the Czech Republic. Mutation research 2009 Jun 666 (1-2): 64-7. Pardini Barbara, Naccarati Alessio, Polakova Veronika, Smerhovsky Zdenek, Hlavata Ivona, Soucek Pavel, Novotny Jan, Vodickova Ludmila, Tomanova Vera, Landi Stefano, Vodicka Pav |
| Heterozygous germ-line mutations in the NBN gene predispose to medulloblastoma in pediatric patients. Acta neuropathologica 2010 Mar 119 (3): 325-34. Ciara El?bieta, Piekutowska-Abramczuk Dorota, Popowska Ewa, Grajkowska Wies?awa, Barszcz S?awomir, Perek Danuta, Dembowska-Bagi?ska Bo?enna, Perek-Polnik Marta, Kowalewska Ewa, Czaj?ska Aneta, Syczewska Ma?gorzata, Czornak Kamila, Krajewska-Walasek Ma?gorzata, Roszkowski Marcin, Chrzanowska Krystyna |
| High prevalence of the NBN gene mutation c.657-661del5 in Southeast Germany. Journal of applied genetics 2010 51 (2): 211-4. Maurer M H, Hoffmann K, Sperling K, Varon |
| Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population. Leukemia research 2011 Nov 35 (11): 1534-6. Pastorczak Agata, Górniak Patryk, Sherborne Amy, Hosking Fay, Treli?ska Joanna, Lejman Monika, Szczepa?ski Tomasz, Borowiec Maciej, Fendler Wojciech, Kowalczyk Jerzy, Houlston Richard S, M?ynarski Wojcie |
| [Heterozygous carriers of Slavic mutation 657del5 of NBN gene in patients with colorectal cancer]. Casopís lékar?? c?eských 2011 150 (2): 97-9. Seemanová Eva, Hoch Jirí, Seeman Pav |
| Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer. Familial cancer 2012 Aug . Zuhlke KA, Johnson AM, Okoth LA, Stoffel EM, Robbins CM, Tembe WA, Salinas CA, Zheng SL, Xu J, Carpten JD, Lange EM, Isaacs WB, Cooney KA |
| Germline Genetic NBN Variation and Predisposition to B-cell Acute Lymphoblastic Leukemia in Children. Research square 2023 7 . Jun Yang, Carolin Escherich, Wenan Chen, Yizhen Li, Wenjian Yang, Rina Nishii, Zhenhua Li, Elizabeth Raetz, Meenakshi Devidas, Gang Wu, Kim Nichols, Hiroto Inaba, Ching-Hon Pui, Sima Jeha, Bruce Camitta, Eric Larsen, Stephen Hunger, Mignon L |
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