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Journal Abstract Search

116 related items for PubMed ID: 1687883

  • 41. Familial intracranial aneurysms: recurrence risk and accidental aggregation study.
    Mathieu J, Hébert G, Pérusse L, Prévost C, Cantin L, Bouchard JM, DeBraekeleer M.
    Can J Neurol Sci; 1997 Nov; 24(4):326-31. PubMed ID: 9398980
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  • 42. Population history and its impact on medical genetics in Quebec.
    Laberge AM, Michaud J, Richter A, Lemyre E, Lambert M, Brais B, Mitchell GA.
    Clin Genet; 2005 Oct; 68(4):287-301. PubMed ID: 16143014
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  • 43. Two novel 1alpha-hydroxylase mutations in French-Canadians with vitamin D dependency rickets type I1.
    Yoshida T, Monkawa T, Tenenhouse HS, Goodyer P, Shinki T, Suda T, Wakino S, Hayashi M, Saruta T.
    Kidney Int; 1998 Nov; 54(5):1437-43. PubMed ID: 9844119
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  • 44. 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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  • 46. [Hereditary tyrosinemia and vitamin-dependent rickets in Saguenay. A genetic and demographic approach].
    Bouchard G, Laberge C, Scriver CR.
    Union Med Can; 1985 Aug 11; 114(8):633-6. PubMed ID: 4060342
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  • 50. Vitamin D receptor polymorphisms in hypocalcemic vitamin D-resistant rickets carriers.
    Nicolaidou P, Papadopoulou A, Matsinos YG, Georgouli H, Fretzayas A, Papadimitriou A, Priftis K, Douros K, Chrousos GP.
    Horm Res; 2007 Aug 11; 67(4):179-83. PubMed ID: 17106204
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  • 51. [Association of the vitamin D receptor gene start codon polymorphism with vitamin D deficiency rickets].
    Lu HJ, Li HL, Hao P, Li JM, Zhou LF.
    Zhonghua Er Ke Za Zhi; 2003 Jul 11; 41(7):493-6. PubMed ID: 14746673
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  • 54. The intron 7 donor splice site transition: a second Tay-Sachs disease mutation in French Canada.
    Hechtman P, Boulay B, De Braekeleer M, Andermann E, Melançon S, Larochelle J, Prevost C, Kaplan F.
    Hum Genet; 1992 Dec 11; 90(4):402-6. PubMed ID: 1483696
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  • 55. Variability of the genetic contribution of Quebec population founders associated to some deleterious genes.
    Heyer E, Tremblay M.
    Am J Hum Genet; 1995 Apr 11; 56(4):970-8. PubMed ID: 7717408
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  • 60. [Association of the vitamin D receptor gene start codon polymorphism with delayed rickets].
    Lu JJ, Li YN, Jin Y, Li L.
    Zhonghua Er Ke Za Zhi; 2007 Jan 11; 45(1):46-9. PubMed ID: 17349151
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