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Journal Abstract Search

116 related items for PubMed ID: 1687883

  • 21.
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  • 23. 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
    [Abstract] [Full Text] [Related]

  • 24. Hereditary disorders in Saguenay-Lac-St-Jean (Quebec, Canada).
    De Braekeleer M.
    Hum Hered; 1991 Jan; 41(3):141-6. PubMed ID: 1937486
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  • 28. 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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  • 29. Mapping autosomal recessive vitamin D dependency type I to chromosome 12q14 by linkage analysis.
    Labuda M, Morgan K, Glorieux FH.
    Am J Hum Genet; 1990 Jul 01; 47(1):28-36. PubMed ID: 1971995
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  • 30. Geographic distribution and genealogy of mutation 207 of the lipoprotein lipase gene in the French Canadian population of Québec.
    Normand T, Bergeron J, Fernandez-Margallo T, Bharucha A, Ven Murthy MR, Julien P, Gagné C, Dionne C, De Braekeleer M, Ma R.
    Hum Genet; 1992 Aug 01; 89(6):671-5. PubMed ID: 1511985
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  • 31. Evidence of a founder effect for the protein C gene 3363 inserted C mutation in thrombophilic pedigrees of French origin.
    Couture P, Bovill EG, Demers C, Simard J, Delage R, Scott BT, Valliere JE, Callas PW, Jomphe M, Rosendaal FR, Aiach M, Long GL.
    Thromb Haemost; 2001 Oct 01; 86(4):1000-6. PubMed ID: 11686315
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  • 32. A study of inbreeding and kinship in intracranial aneurysms in the Saguenay Lac-Saint-Jean region (Quebec, Canada).
    De Braekeleer M, Pérusse L, Cantin L, Bouchard JM, Mathieu J.
    Ann Hum Genet; 1996 Mar 01; 60(2):99-104. PubMed ID: 8839125
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  • 34. Founder effect in familial hyperchylomicronemia among French Canadians of Quebec.
    De Braekeleer M, Dionne C, Gagné C, Julien P, Brun D, Ven Murthy MR, Lupien PJ.
    Hum Hered; 1991 Mar 01; 41(3):168-73. PubMed ID: 1937490
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  • 35. The French Canadian Tay-Sachs disease deletion mutation: identification of probable founders.
    De Braekeleer M, Hechtman P, Andermann E, Kaplan F.
    Hum Genet; 1992 Apr 01; 89(1):83-7. PubMed ID: 1577470
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  • 36. Geographic distribution of French-Canadian low-density lipoprotein receptor gene mutations in the Province of Quebec.
    Vohl MC, Moorjani S, Roy M, Gaudet D, Torres AL, Minnich A, Gagné C, Tremblay G, Lambert M, Bergeron J, Couture P, Perron P, Blaichman S, Brun LD, Davignon J, Lupien PJ, Després JP.
    Clin Genet; 1997 Jul 01; 52(1):1-6. PubMed ID: 9272705
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  • 37. Consanguinity and kinship in Down syndrome in Saguenay Lac-Saint-Jean (Québec).
    de Braekeleer M, Landry T, Cholette A.
    Ann Genet; 1994 Jul 01; 37(2):86-8. PubMed ID: 7985984
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  • 38. Seventeenth-century European origins of hereditary diseases in the Saguenay population (Quebec, Canada).
    Heyer E, Tremblay M, Desjardins B.
    Hum Biol; 1997 Apr 01; 69(2):209-25. PubMed ID: 9057345
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  • 39. [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 Apr 01; 148(10):601-4. PubMed ID: 1295054
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  • 40. Prevalence, geographical distribution and genealogical investigations of mutation 188 of lipoprotein lipase gene in the French Canadian population of Québec.
    Bergeron J, Normand T, Bharucha A, Ven Murthy MR, Julien P, Gagné C, Dionne C, De Braekeleer M, Brun D, Hayden MR.
    Clin Genet; 1992 Apr 01; 41(4):206-10. PubMed ID: 1576758
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