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Novel founder mutation in French-Canadian families with Naxos disease.
Marino TC, Maranda B, Leblanc J, Pratte A, Barabas M, Dupéré A, Lévesque S. Marino TC, et al. Among authors: leblanc j. Clin Genet. 2017 Oct;92(4):451-453. doi: 10.1111/cge.12971. Epub 2017 Feb 22. Clin Genet. 2017. PMID: 28098346 No abstract available.
A Collaborative Model to Implement Flexible, Accessible and Efficient Oncogenetic Services for Hereditary Breast and Ovarian Cancer: The C-MOnGene Study.
Lapointe J, Dorval M, Chiquette J, Joly Y, Guertin JR, Laberge M, Gekas J, Hébert J, Pomey MP, Cruz-Marino T, Touhami O, Blanchet Saint-Pierre A, Gagnon S, Bouchard K, Rhéaume J, Boisvert K, Brousseau C, Castonguay L, Fortier S, Gosselin I, Lachapelle P, Lavoie S, Poirier B, Renaud MC, Ruizmangas MG, Sebastianelli A, Roy S, Côté M, Racine MM, Roy MC, Côté N, Brisson C, Charette N, Faucher V, Leblanc J, Dubeau MÈ, Plante M, Desbiens C, Beaumont M, Simard J, Nabi H. Lapointe J, et al. Among authors: leblanc j. Cancers (Basel). 2021 May 31;13(11):2729. doi: 10.3390/cancers13112729. Cancers (Basel). 2021. PMID: 34072979 Free PMC article.
1,228 results