Cancer: dermatological

Germline CHEK2*1100delC mutations in breast cancer patients with multiple primary cancers
J Huang, S M Domchek, M S Brose, T R Rebbeck, K L Nathanson, B L Weber

Journal of Medical Genetics Nov 2004, 41 (11) e120; DOI: 10.1136/jmg.2004.022913
Genetic susceptibility in familial melanoma from northeastern Italy
M T Landi, A M Goldstein, S Tsang, D Munroe, W Modi, M Ter-Minassian, R Steighner, M Dean, N Metheny, B Staats, R Agatep, D Hogg, D Calista

Journal of Medical Genetics Jul 2004, 41 (7) 557-566; DOI: 10.1136/jmg.2003.016907
A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome
E Mangold, C Pagenstecher, M Leister, M Mathiak, A Rütten, W Friedl, P Propping, T Ruzicka, R Kruse

Journal of Medical Genetics Jul 2004, 41 (7) 567-572; DOI: 10.1136/jmg.2003.012997
Prospective risk of cancer in CDKN2A germline mutation carriers
A M Goldstein, J P Struewing, M C Fraser, M W Smith, M A Tucker

Journal of Medical Genetics Jun 2004, 41 (6) 421-424; DOI: 10.1136/jmg.2004.019349
Significant involvement of CCR2–64I and CXCL12–3a in the development of sporadic breast cancer
A Zafiropoulos, N Crikas, A M Passam, D A Spandidos

Journal of Medical Genetics May 2004, 41 (5) e59; DOI: 10.1136/jmg.2003.013649
Absence of BRAF mutations in UV-protected mucosal melanomas
R H Edwards, M R Ward, H Wu, C A Medina, M S Brose, P Volpe, S Nussen-Lee, H M Haupt, A M Martin, M Herlyn, S R Lessin, B L Weber

Journal of Medical Genetics Apr 2004, 41 (4) 270-272; DOI: 10.1136/jmg.2003.016667
Extending the p16-Leiden tumour spectrum by respiratory tract tumours
R A Oldenburg, W H de Vos tot Nederveen Cappel, M van Puijenbroek, A van den Ouweland, E Bakker, G Griffioen, P Devilee, C J Cornelisse, H Meijers-Heijboer, H F A Vasen, H Morreau

Journal of Medical Genetics Mar 2004, 41 (3) e31; DOI: 10.1136/jmg.2003.012336
Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure
E Matichard, P Verpillat, R Meziani, B Gérard, V Descamps, E Legroux, M Burnouf, G Bertrand, F Bouscarat, A Archimbaud, C Picard, L Ollivaud, N Basset-Seguin, D Kerob, G Lanternier, C Lebbe, B Crickx, B Grandchamp, N Soufir

Journal of Medical Genetics Feb 2004, 41 (2) e13; DOI: 10.1136/jmg.2003.011536
Identification of a splice acceptor site mutation in p16^INK4A/p14^ARF within a breast cancer, melanoma, neurofibroma prone kindred
A H Prowse, D C Schultz, S Guo, L Vanderveer, J Dangel, B Bove, P Cairns, M Daly, A K Godwin

Journal of Medical Genetics Aug 2003, 40 (8) e102; DOI: 10.1136/jmg.40.8.e102
Germline TP53 mutations in breast cancer families with multiple primary cancers: is TP53 a modifier of BRCA1?
A-M Martin, P A Kanetsky, B Amirimani, T A Colligon, G Athanasiadis, H A Shih, M R Gerrero, K Calzone, T R Rebbeck, B L Weber

Journal of Medical Genetics Apr 2003, 40 (4) e34; DOI: 10.1136/jmg.40.4.e34

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