An abnormal concentration of cases of Rendu-Osler disease in the Valserine valley of the French Jura: a genealogical and demographic study

References

• Bideau A., Brunet G., Heyer E., Plauchu H. Histoire généalogique ou généalogie historique: constitution de la population de la vallée de la Valserine. Manuscript accepted for publication. 1991
   Google Scholar
• Bideau A., Desjardins B., Brunet G., Legare J. Démographie historique et génétique de population: collaboration franco-québécoise autour de la constitution de registres de populations. Populations et Culture. Rennes Université de Rennes. 1989; 9–20, In
   Google Scholar
• Bideau A., Plauchu H., Brunet G., Robert J.M. Epidémiologie d'une maladie héréditaire rare en France. Mutation ou diffusion d'un gene pathologique. Population 1989; 1: 9–28
   Web of Science ®Google Scholar
• Bideau A., Plauchu H., Jacquard A. Démographie Historique et génétique des populations: la concentration géographique d'une maladie héréditaire rare. Annales Economie, Société et Civilisation 1979; 34: 85–105
   PubMedGoogle Scholar
• Bouchard J.P., Gagne F., Tome F., Brunet D. Nuclear inclusions in oculopharyngeal muscular dystrophy in Quebec. Canadian Journal of Neurological Sciences 1989; 16(4)446–450
   PubMed Web of Science ®Google Scholar
• Bouchard G., Roy R., Declos M., Kouladjian K., Mathieu J. La diffusion du g`ene de la dystrophie myotonique au Saguenay (Québec). Journal de Génétique Humaine 1988; 36: 221–237
   PubMedGoogle Scholar
• Brunet G. Dictionnaire d'histoire administrative et démographique du département de l'Ain. CNRS, Paris 1978; 578–578
   Google Scholar
• Charbonneau H., Desjardins B., Guillemette A., Landry Y., Legare J., Nault F. Naissance d'une population. Les francais établis au Canada au 17e si`ecle. INED, Paris 1987; 232–232
   Google Scholar
• Crawford, M.H. The breakdown of reproductive isolation in an Alpine isolate: Aceglio, Italy. Population Structure and Genetic Disorders, A.W. Eriksson, et al. Academic Press, London 1980; 57–72, In
   Google Scholar
• De Braekeleer M., Mathieu J. Genealogical reconstruction of myotonic dystrophy in the Saguenay region. De la dynamique de la population `a l'épidemiologie génétique, G. Bouchard. SOREP, Chicoutimi 1988; 303–314, In
   Google Scholar
• Dodinval P., Klein D. Caract`eres démographiques et génétiques d'un petit village savoyard. Journal de Génétique Humaine 1962; 11: 1–15
   PubMedGoogle Scholar
• Hagaman R.M., Ellis W.S., Netting R.M. The genetic and demographic impact of immigrants in a largely endogamous community. Annals of Human Biology 1978; 5(6)505–515
   PubMed Web of Science ®Google Scholar
• Heyer E. Etude démogénétique d'une population humaine. Cas de la maladie de Rendu-Osler. Th`ese de Science. Lyon 1991; 194–194
   Google Scholar
• Jacquard A. The Genetic Structure of Populations. Springer Verlag, Berlin 1970; 569–569
   Google Scholar
• Kere J., Norio R., Savilahti E., Estivill X., De La Chapelle A. Cystic fibrosis in Finland: a molecular and genealogical study. Human Genetics 1989; 83: 20–25
   PubMed Web of Science ®Google Scholar
• Kucheman C.F., Boyce A.J., Harrison G.A. A demographic and genetic study of a group of Oxfordshire villages. Human Biology 1967; 39: 251–276
   Web of Science ®Google Scholar
• Lasker G.W., Chiarelli B., Masali M., Fedele F., Kaplan B.A. Degree of human genetic isolation measured by isonymy and marital distance in two communities in an Alpine valley. Human Biology 1972; 44: 351–360
   PubMed Web of Science ®Google Scholar
• Lehy J.Y. L'angiomatose de Rendu-Osler. Etude démographique et génétique dans le département des Deux-Sevres. Th`ese de médecine. Nantes 1983; 164–164
   Google Scholar
• Manipoud J.P. Contribution `a l'étude de la maladie de Rendu-Osler `a propos de 37 observations. Th`ese de médecine. Lyon 1962; 123–123, (Cas compilés dans le service de Génétique du Pr J.M. Robert, Lyon)
   Google Scholar
• Maszelin P. Etude clinique, géographique et généalogique `a partir de 51 proposants de Rendu-Osler recensés dans cinq départements de l'Est du Massif Central. Th`ese de médecine. Lyon 1990; 290–290
   Google Scholar
• Nordstrom S., Barkman Y. Hereditary macular degeneration in 246 cases traced to one gene source in central Sweden. Hereditas 1976; 84: 163–176
   Web of Science ®Google Scholar
• Nordstrom S., Polland W. Different expressions of one gene for congenital Achromatopsia with Amblyopia in northern Sweden. Human Heredity 1980; 30: 122–128
   PubMed Web of Science ®Google Scholar
• O'Brien E., Jorde L.B., Ronnlof B., Fellman J.O., Eriksson A.W. Inbreeding and genetic disease in Sottunga, Finland. American Journal of Physical Anthropology 1988a; 75: 477–486
   PubMed Web of Science ®Google Scholar
• O'Brien E., Jorde L.B., Ronnlof B., Fellman J.O., Eriksson A.W. Founder effect and genetic disease in Sottunga, Finland. American Journal of Physical Anthropology 1988b; 77: 335–346
   PubMed Web of Science ®Google Scholar
• Osler W. On a family form of recurring epistaxis, associated with multiple telangiectases of the skin and mucous membranes. Bulletin of the Johns Hopkins Hospital 1901; 12: 333–337
   Google Scholar
• Plauchu H., De Chadarevian J.P., Bideau A., Robert J.M. Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population. American Journal of Medical Genetics 1989; 32: 291–297
   PubMed Web of Science ®Google Scholar
• Poulard S., Heyer E., Guillemette A., Brunet G. SYGAP syst`eme de gestion et d'analyse de populations. PPSH, Lyon 1991, p. 235 + diskette
   Google Scholar
• Rendu H. Epistaxis répétées chez un sujet porteur de petits angiomes cutanes et muqueux. Gazette des Hopitaux (Paris) 1896; 135: 132–133
   Google Scholar
• Roberts D.F., Mohan M. History, demography and genetics: the Fiji experience and its evolutionary implications. Demographic Evolution of Human Populations, R.H. Ward, K.M. Weiss. Academic Press, London 1976; 117–128, in
   Google Scholar
• Sankila E.M., De La Chapelle A., Karna J., Forsius H., Frants R., Eriksson A. Choroideremia: close linkage to DXYS1 and DXYS12 demonstrated by segregation analysis and historical-genealogical evidence. Clinical Genetics 1987; 31: 315–322
   PubMed Web of Science ®Google Scholar
• Serre J.L., Jakobi L., Barron M.C. A genetic isolate in the French Pyrenees: probabilities of origin of genes and inbreeding. Journal of Biosocial Science 1985; 17: 405–414
   PubMed Web of Science ®Google Scholar
• Thompson E.A. Pedigree Analysis in Human Genetics. Johns Hopkins University Press, Baltimore 1986; 213–213
   Google Scholar
• Thompson E.A., Morgan K. Recessive descent probabilities for rare recessive lethals. Annals of Human Genetics 1989; 53: 357–374
   PubMed Web of Science ®Google Scholar