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Journal Abstract Search

110 related items for PubMed ID: 8215233

  • 21. Inbreeding and kinship in Saguenay-Lac-St-Jean: a study of newborn samples 1956-1971.
    De Braekeleer M.
    Ann Hum Biol; 1992; 19(2):115-24. PubMed ID: 1580536
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  • 22. Exploring rare and low-frequency variants in the Saguenay-Lac-Saint-Jean population identified genes associated with asthma and allergy traits.
    Morin A, Madore AM, Kwan T, Ban M, Partanen J, Rönnblom L, Syvänen AC, Sawcer S, Stunnenberg H, Lathrop M, Pastinen T, Laprise C.
    Eur J Hum Genet; 2019 Jan; 27(1):90-101. PubMed ID: 30206357
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  • 23. Haemochromatosis mutations in North-East Scotland.
    Miedzybrodzka Z, Loughlin S, Baty D, Terron A, Kelly K, Dean J, Greaves M, Pippard M, Haites N.
    Br J Haematol; 1999 Aug; 106(2):385-7. PubMed ID: 10460595
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  • 24. [Preliminary results on the residence distribution at birth of patients with Alzheimer's disease in the Saguenay-Lac-Saint-Jean/Quebec (the IMAGE project)].
    Emard JF, Thouez JP, Mathieu J, Boily C, Beaudry M, Cholette A, Robitaille Y, Bouchard R, Gauvreau D.
    Cah Sociol Demogr Med; 1992 Aug; 32(1):51-77. PubMed ID: 1638449
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  • 25. Cystic fibrosis mutations in French Canadians: three CFTR mutations are relatively frequent in a Quebec population with an elevated incidence of cystic fibrosis.
    Rozen R, De Braekeleer M, Daigneault J, Ferreira-Rajabi L, Gerdes M, Lamoureux L, Aubin G, Simard F, Fujiwara TM, Morgan K.
    Am J Med Genet; 1992 Feb 01; 42(3):360-4. PubMed ID: 1536179
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  • 26. 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.
    Hum Genet; 2005 Jul 01; 117(2-3):177-87. PubMed ID: 15883838
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  • 29. Genetic burden linked to founder effects in Saguenay-Lac-Saint-Jean illustrates the importance of genetic screening test availability.
    Bchetnia M, Bouchard L, Mathieu J, Campeau PM, Morin C, Brisson D, Laberge AM, Vézina H, Gaudet D, Laprise C.
    J Med Genet; 2021 Oct 01; 58(10):653-665. PubMed ID: 33910931
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  • 30. Demogenetic study of three populations within a region with strong founder effects.
    Lavoie EM, Tremblay M, Houde L, Vézina H.
    Community Genet; 2005 Oct 01; 8(3):152-60. PubMed ID: 16113532
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  • 34. Prevalence of the C282Y mutation for haemochromatosis on the Island of Majorca.
    Guix P, Picornell A, Parera M, Tomás C, Muncunill J, Castro JA, Rossell J, Vaquer P, Ramon MM, Obrador A.
    Clin Genet; 2000 Aug 01; 58(2):123-8. PubMed ID: 11005145
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  • 35. A single mutation of the fumarylacetoacetate hydrolase gene in French Canadians with hereditary tyrosinemia type I.
    Grompe M, St-Louis M, Demers SI, al-Dhalimy M, Leclerc B, Tanguay RM.
    N Engl J Med; 1994 Aug 11; 331(6):353-7. PubMed ID: 8028615
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  • 37. Complete identification of cystic fibrosis transmembrane conductance regulator mutations in the CF population of Saguenay Lac-Saint-Jean (Quebec, Canada).
    De Braekeleer M, Mari C, Verlingue C, Allard C, Leblanc JP, Simard F, Aubin G, Férec C.
    Clin Genet; 1998 Jan 11; 53(1):44-6. PubMed ID: 9550360
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  • 38. Fertility in couples heterozygous for the tyrosinemia gene in Saguenay Lac-St-Jean.
    De Braekeleer M, Lamarre V, Scriver CR, Larochelle J, Bouchard G.
    Genet Couns; 1990 Jan 11; 1(3-4):259-64. PubMed ID: 2098050
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  • 40. [Genealogical study of oculopharyngeal dystrophy at Saguenay-Lac-St-Jean, Quebec, Canada].
    Tremblay-Tymczuk S, Mathieu J, Morgan K, Bouchard JP, De Braekeleer M.
    Rev Neurol (Paris); 1992 Jan 11; 148(10):601-4. PubMed ID: 1295054
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