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Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families.
Phelan CM, Lancaster JM, Tonin P, Gumbs C, Cochran C, Carter R, Ghadirian P, Perret C, Moslehi R, Dion F, Faucher MC, Dole K, Karimi S, Foulkes W, Lounis H, Warner E, Goss P, Anderson D, Larsson C, Narod SA, Futreal PA. Phelan CM, et al. Among authors: faucher mc. Nat Genet. 1996 May;13(1):120-2. doi: 10.1038/ng0596-120. Nat Genet. 1996. PMID: 8673090
Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markers.
Ruttledge MH, Narod SA, Dumanski JP, Parry DM, Eldridge R, Wertelecki W, Parboosingh J, Faucher MC, Lenoir GM, Collins VP, et al. Ruttledge MH, et al. Among authors: faucher mc. Neurology. 1993 Sep;43(9):1753-60. doi: 10.1212/wnl.43.9.1753. Neurology. 1993. PMID: 8414026
HLA-G Alleles Impact the Perinatal Father-Child HPV Transmission.
Suominen NT, Roger M, Faucher MC, Syrjänen KJ, Grénman SE, Syrjänen SM, Louvanto K. Suominen NT, et al. Among authors: faucher mc. Curr Issues Mol Biol. 2023 Jul 12;45(7):5798-5810. doi: 10.3390/cimb45070366. Curr Issues Mol Biol. 2023. PMID: 37504282 Free PMC article.
19 results