Free Access
Issue |
Med Sci (Paris)
Volume 23, Number 11, Novembre 2007
|
|
---|---|---|
Page(s) | 997 - 1001 | |
Section | M/S revues | |
DOI | https://doi.org/10.1051/medsci/20072311997 | |
Published online | 15 November 2007 |
- De Braekeleer M, Dao TN. Hereditary disorders in the French Canadian population of Quebec. I. In search of founders. Hum Biol 1994; 66 : 205–23. [Google Scholar]
- De Braekeleer M, Dao TN. Hereditary disorders in the French Canadian population of Quebec. II. Contribution of Perche. Hum Biol 1994; 66 : 225–49. [Google Scholar]
- Charbonneau H, Desjardins B, Guillemette A, et al. Naissance d’une population : les Français établis au Canada au xviie siècle. Paris et Montréal : Presses Universitaires de France et Presses de l’Université de Montréal, 1987 : 232 p. [Google Scholar]
- Larin R. Brève histoire du peuplement européen en Nouvelle-France. Sillery : Éditions du Septentrion, 2000 : 226 p. [Google Scholar]
- Institut de la Statistique du Québec. Recensement de la population 1996-1991-1986. Données comparatives et faits saillants. Cahier 3. Immigration, langue et origine ethnique. Publications du Québec, 1999 : 158 p. [Google Scholar]
- McGowan-Jordan J, Stoddard K, Podolsky L, et al. Molecular analysis of cystinosis : probable Irish origin of the most common French Canadian mutation. Eur J Hum Genet 1999; 7 : 671–8. [Google Scholar]
- Brittingham A, de la Cruz GP. Ancestry : 2000. Census 2000 brief. US Census Bureau, 2004 : 10. [Google Scholar]
- Strachan T, Read AP. Human molecular genetics 3. 2nd ed. New York : Wiley-Liss, 2004; 576 : XXIII. [Google Scholar]
- Bouchard G, De Braekeleer M. Histoire d’un génome : population et génétique dans l’est du Québec. Sillery : Presses de l’Université du Québec, 1991 : 607. [Google Scholar]
- Laberge AM, Michaud J, Richter A, et al. Population history and its impact on medical genetics in Quebec. Clin Genet 2005; 68 : 287–301. [Google Scholar]
- Scriver CR. Human genetics : lessons from Quebec populations. Annu Rev Genomics Hum Genet 2001; 2 : 69–101. [Google Scholar]
- Engert JC, Berube P, Mercier J, et al. ARSACS, a spastic ataxia common in northeastern Quebec, is caused by mutations in a new gene encoding an 11.5-kb ORF. Nat Genet 2000; 24 : 120–5. [Google Scholar]
- Dupré N, Howard HC, Mathieu J, et al. Hereditary motor and sensory neuropathy with agenesis of the corpus callosum. Ann Neurol 2003; 54 : 9–18. [Google Scholar]
- De Braekeleer M, Larochelle J. Genetic epidemiology of hereditary tyrosinemia in Quebec and in Saguenay-Lac-St-Jean. Am J Hum Genet 1990; 47 : 302–7. [Google Scholar]
- Brais B, Rouleau GA, Bouchard JP, et al. Oculopharyngeal muscular dystrophy. Semin Neurol 1999; 19 : 59–66. [Google Scholar]
- Carter K, Byck S, Waters P, et al. Mutation at the phenylalanine hydroxylase gene (PAH) and its use to document population genetic variation : the Quebec experience. Eur J Hum Genet 1998; 6 : 61–70. [Google Scholar]
- Chappuis PO, Hamel N, Paradis AJ, et al. Prevalence of founder BRCA1 and BRCA2 mutations in unselected French Canadian women with breast cancer. Clin Genet 2001; 59 : 418–23. [Google Scholar]
- Tonin PN, Perret C, Lambert JA, et al. Founder BRCA1 and BRCA2 mutations in early-onset French Canadian breast cancer cases unselected for family history. Int J Cancer 2001; 95 : 189–93. [Google Scholar]
- Merante F, Petrova-Benedict R, MacKay N, et al. A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec. Am J Hum Genet 1993; 53 : 481–7. [Google Scholar]
- Kaplan F, Kokotsis G, DeBraekeleer M, et al. Beta-thalassemia genes in French-Canadians : haplotype and mutation analysis of Portneuf chromosomes. Am J Hum Genet 1990; 46 : 126–32. [Google Scholar]
- Vohl MC, Moorjani S, Roy M, et al. Geographic distribution of French-Canadian low-density lipoprotein receptor gene mutations in the Province of Quebec. Clin Genet 1997; 52 : 1–6. [Google Scholar]
- Zlotogora J. Knowing the ethnic origin of the patient is important in making a diagnosis. Am J Med Genet 1998; 78 : 393–4. [Google Scholar]
- Bouchard JP, Richter A, Melancon SB, et al. Autosomal recessive spastic ataxia (Charlevoix-Saguenay). In : Klockgether T, ed. Handbook of ataxia disorders. New York : Marcel Dekker, 2000 : 311–24. [Google Scholar]
- Poudrier J, St-Louis M, Lettre F, et al. Frequency of the IVS12 + 5G ® A splice mutation of the fumarylacetoacetate hydrolase gene in carriers of hereditary tyrosinaemia in the French Canadian population of Saguenay-Lac-St-Jean. Prenat Diagn 1996; 16 : 59–64. [Google Scholar]
- Palomaki GE, FitzSimmons SC, Haddow JE. Clinical sensitivity of prenatal screening for cystic fibrosis via CFTR carrier testing in a United States panethnic population. Genet Med 2004; 6 : 405–14. [Google Scholar]
- El Euch-Fayache G, Lalani I, Amouri R, et al. Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia. Arch Neurol 2003; 60 : 982–8. [Google Scholar]
- Criscuolo C, Banfi S, Orio M, et al. A novel mutation in SACS gene in a family from southern Italy. Neurology 2004; 62 : 100–2. [Google Scholar]
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.