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A polymorphic stop codon in BRCA2.
Mazoyer S, Dunning AM, Serova O, Dearden J, Puget N, Healey CS, Gayther SA, Mangion J, Stratton MR, Lynch HT, Goldgar DE, Ponder BA, Lenoir GM. Mazoyer S, et al. Among authors: lynch ht. Nat Genet. 1996 Nov;14(3):253-4. doi: 10.1038/ng1196-253. Nat Genet. 1996. PMID: 8896551 No abstract available.
A large multisite cancer family is linked to BRCA2.
Tonin P, Ghadirian P, Phelan C, Lenoir GM, Lynch HT, Letendre F, Belanger D, Monté M, Narod SA. Tonin P, et al. Among authors: lynch ht. J Med Genet. 1995 Dec;32(12):982-4. doi: 10.1136/jmg.32.12.982. J Med Genet. 1995. PMID: 8825930 Free PMC article.
BRCA2 hereditary breast cancer pathophenotype.
Marcus JN, Watson P, Page DL, Narod SA, Tonin P, Lenoir GM, Serova O, Lynch HT. Marcus JN, et al. Among authors: lynch ht. Breast Cancer Res Treat. 1997 Jul;44(3):275-7. doi: 10.1023/a:1005830230664. Breast Cancer Res Treat. 1997. PMID: 9266108 No abstract available.
A BRCA1 nonsense mutation causes exon skipping.
Mazoyer S, Puget N, Perrin-Vidoz L, Lynch HT, Serova-Sinilnikova OM, Lenoir GM. Mazoyer S, et al. Among authors: lynch ht. Am J Hum Genet. 1998 Mar;62(3):713-5. doi: 10.1086/301768. Am J Hum Genet. 1998. PMID: 9497265 Free PMC article. No abstract available.
Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers.
Chenevix-Trench G, Sinilnikova OM, Suthers G, Pandeya N, Mazoyer S, Sambrook JF, Goldup S, Goldgar D, Lynch HT, Lenoir GM, Cheetham G; kConFab. Chenevix-Trench G, et al. Among authors: lynch ht. Fam Cancer. 2005;4(2):73-5. doi: 10.1007/s10689-004-2102-y. Fam Cancer. 2005. PMID: 15951955
An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation?
Puget N, Sinilnikova OM, Stoppa-Lyonnet D, Audoynaud C, Pagès S, Lynch HT, Goldgar D, Lenoir GM, Mazoyer S. Puget N, et al. Among authors: lynch ht. Am J Hum Genet. 1999 Jan;64(1):300-2. doi: 10.1086/302211. Am J Hum Genet. 1999. PMID: 9915971 Free PMC article. No abstract available.
854 results