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Page 1
Joubert Syndrome in French Canadians and Identification of Mutations in CEP104.
Srour M, Hamdan FF, McKnight D, Davis E, Mandel H, Schwartzentruber J, Martin B, Patry L, Nassif C, Dionne-Laporte A, Ospina LH, Lemyre E, Massicotte C, Laframboise R, Maranda B, Labuda D, Décarie JC, Rypens F, Goldsher D, Fallet-Bianco C, Soucy JF, Laberge AM, Maftei C; Care4Rare Canada Consortium; Boycott K, Brais B, Boucher RM, Rouleau GA, Katsanis N, Majewski J, Elpeleg O, Kukolich MK, Shalev S, Michaud JL. Srour M, et al. Among authors: labuda d. Am J Hum Genet. 2015 Nov 5;97(5):744-53. doi: 10.1016/j.ajhg.2015.09.009. Epub 2015 Oct 17. Am J Hum Genet. 2015. PMID: 26477546 Free PMC article.
[Founder effects and genetic variability in Quebec].
Moreau C, Vézina H, Labuda D. Moreau C, et al. Among authors: labuda d. Med Sci (Paris). 2007 Nov;23(11):1008-13. doi: 10.1051/medsci/200723111008. Med Sci (Paris). 2007. PMID: 18021716 Free article. French.
Ethiopia: between Sub-Saharan Africa and western Eurasia.
Lovell A, Moreau C, Yotova V, Xiao F, Bourgeois S, Gehl D, Bertranpetit J, Schurr E, Labuda D. Lovell A, et al. Among authors: labuda d. Ann Hum Genet. 2005 May;69(Pt 3):275-87. doi: 10.1046/j.1529-8817.2005.00152.x. Ann Hum Genet. 2005. PMID: 15845032
Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec.
Yotova V, Labuda D, Zietkiewicz E, Gehl D, Lovell A, Lefebvre JF, Bourgeois S, Lemieux-Blanchard E, Labuda M, Vézina H, Houde L, Tremblay M, Toupance B, Heyer E, Hudson TJ, Laberge C. Yotova V, et al. Among authors: labuda m, labuda d. Hum Genet. 2005 Jul;117(2-3):177-87. doi: 10.1007/s00439-005-1298-8. Epub 2005 May 10. Hum Genet. 2005. PMID: 15883838
182 results