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Annals of Human Biology Volume 22, 1995 - Issue 2
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Original Article

Geographic distribution of 18 autosomal recessive disorders in the French Canadian population of Saguenay-Lac-Saint-Jean, Quebec

M. De Braekeleer Université du Québec à Chicoutimi, Chicoutimi, Québec, Canada
Pages 111-122 | Received 20 Aug 1994, Published online: 09 Jul 2009

Citations (11)

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Read on this site (2)

M. De Braekeleer, J. Daigneault, C. Allard, F. Simard & G. Aubin. (1996) Genealogy and geographical distribution of CFTR mutations in Saguenay Lac-Saint-Jean (Quebec, Canada). Annals of Human Biology 23:5, pages 345-352.
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M. De Braekeleer. (1996) Autosomal recessive disorders in Saguenay-Lac-Saint-Jean (Quebec, Canada): estimation of inbreeding from isonymy. Annals of Human Biology 23:2, pages 95-99.
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Articles from other publishers (9)

A‐M Laberge, J Michaud, A Richter, E Lemyre, M Lambert, B Brais & GA Mitchell. (2005) Population history and its impact on medical genetics in Quebec. Clinical Genetics 68:4, pages 287-301.
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Audrey Bilodeau, Pascale Prasil, Raymond Cloutier, Rachel Laframboise, Ari-Nareg Meguerditchian, Guy Roy, Suzanne Leclerc & Jean Péloquin. (2004) Hereditary multiple intestinal atresia: thirty years later. Journal of Pediatric Surgery 39:5, pages 726-730.
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Malcolm T. Smith. 2009. Human Biologists in the Archives. Human Biologists in the Archives 311 336 .
Clara Camaschella, Antonella Roetto & Marco De Gobbi. (2002) Juvenile hemochromatosis. Seminars in Hematology 39:4, pages 242-248.
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Charles R. Scriver. (2001) Human Genetics: Lessons from Quebec Populations. Annual Review of Genomics and Human Genetics 2:1, pages 69-101.
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Jocelyne Mercier, Claude Prévost, James C. Engert, Jean-Pierre Bouchard, Jean Mathieu & Andrea Richter. (2001) Rapid Detection of the Sacsin Mutations Causing Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay. Genetic Testing 5:3, pages 255-259.
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Tarja Laitinen, Mark J. Daly, John D. Rioux, Paula Kauppi, Catherine Laprise, Tuula Petäys, Todd Green, Michele Cargill, Tari Haahtela, Eric S. Lander, Lauri A. Laitinen, Thomas J. Hudson & Juha Kere. (2001) A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population. Nature Genetics 28:1, pages 87-91.
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James C. Engert, Pierre Bérubé, Jocelyne Mercier, Carole Doré, Pierre Lepage, Bing Ge, Jean-Pierre Bouchard, Jean Mathieu, Serge B. Melançon, Martin Schalling, Eric S. Lander, Kenneth Morgan, Thomas J. Hudson & Andrea Richter. (2000) ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF. Nature Genetics 24:2, pages 120-125.
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M. DE BRAEKELEER & S. GAUTHIER. (2007) Autosomal recessive disorders in Saguenay‐Lac‐Saint‐Jean (Quebec, Canada): a study of inbreeding. Annals of Human Genetics 60:1, pages 51-56.
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