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Josué Feingold

Showing results (1-10 of 35) with videos related to

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Medecine Sciences : M/S|November 9, 2005
[Multifactorial diseases: a nightmare for the geneticist]Josué Feingold
La Revue Du Praticien|May 10, 2011
[Genetic counseling for adults: the risk of late-onset inherited diseases]Alexandra Dürr, Josué Feingold
Medecine Sciences : M/S|November 9, 2005
[Predictive testing: presymptomatic diagnosis in neurogenetic disorders]Alexandra Dürr, Marcela Gargiulo, Josué Feingold
Human Biology|April 7, 2006
The Basques: review of population genetics and Mendelian disordersFrédéric Bauduer, Josué Feingold, Didier Lacombe
Human Genetics|September 12, 2008
Identifying modifier genes of monogenic disease: strategies and difficultiesEmmanuelle Génin, Josué Feingold, Françoise Clerget-Darpoux
Comptes Rendus Biologies|January 28, 2006
Prevalence and distribution of MEFV mutations among Arabs from the Maghreb patients suffering from familial Mediterranean feverLatifa Belmahi, Abdelaziz Sefiani, Corinne Fouveau, et al.
Annales De Genetique|April 6, 2002
Linkage disequilibrium and founder effect analysis of the NF1 gene in French Canadians from the Quebec populationLi Juan Fang, Wentian Li, Nader Chalhoub, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 13, 2008
The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonismAgnès Camuzat, Marc Romana, Alexandra Dürr, et al.
Prenatal Diagnosis|September 24, 2004
Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first casePhilippe Charron, Delphine Héron, Marcela Gargiulo, et al.
Brain : a Journal of Neurology|November 14, 2002
A locus for simple pure febrile seizures maps to chromosome 6q22-q24Rima Nabbout, Jean-François Prud'homme, Alexandra Herman, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Medecine Sciences : M/S|November 9, 2005
[Multifactorial diseases: a nightmare for the geneticist]Josué Feingold
La Revue Du Praticien|May 10, 2011
[Genetic counseling for adults: the risk of late-onset inherited diseases]Alexandra Dürr, Josué Feingold
Medecine Sciences : M/S|November 9, 2005
[Predictive testing: presymptomatic diagnosis in neurogenetic disorders]Alexandra Dürr, Marcela Gargiulo, Josué Feingold
Human Biology|April 7, 2006
The Basques: review of population genetics and Mendelian disordersFrédéric Bauduer, Josué Feingold, Didier Lacombe
Human Genetics|September 12, 2008
Identifying modifier genes of monogenic disease: strategies and difficultiesEmmanuelle Génin, Josué Feingold, Françoise Clerget-Darpoux
Comptes Rendus Biologies|January 28, 2006
Prevalence and distribution of MEFV mutations among Arabs from the Maghreb patients suffering from familial Mediterranean feverLatifa Belmahi, Abdelaziz Sefiani, Corinne Fouveau, et al.
Annales De Genetique|April 6, 2002
Linkage disequilibrium and founder effect analysis of the NF1 gene in French Canadians from the Quebec populationLi Juan Fang, Wentian Li, Nader Chalhoub, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 13, 2008
The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonismAgnès Camuzat, Marc Romana, Alexandra Dürr, et al.
Prenatal Diagnosis|September 24, 2004
Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first casePhilippe Charron, Delphine Héron, Marcela Gargiulo, et al.
Brain : a Journal of Neurology|November 14, 2002
A locus for simple pure febrile seizures maps to chromosome 6q22-q24Rima Nabbout, Jean-François Prud'homme, Alexandra Herman, et al.
Pageof 4