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Jean-Louis Serre

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Presse Medicale (Paris, France : 1983)|June 5, 2007
[Various topics in population genetics]Jean-Louis Serre
Molecular Genetics and Metabolism|February 8, 2005
Characterization of 11 novel mutations in the tissue non-specific alkaline phosphatase gene responsible for hypophosphatasia and genotype-phenotype correlationsIsabelle Brun-Heath, Agnes Taillandier, Jean-Louis Serre, et al.
Human Mutation|June 12, 2008
Mutations in TREM2 lead to pure early-onset dementia without bone cystsEliane Chouery, Valérie Delague, Anne Bergougnoux, et al.
European Journal of Human Genetics : EJHG|September 18, 2015
Genome-wide inbreeding estimation within Lebanese communities using SNP arraysNadine Jalkh, Mourad Sahbatou, Eliane Chouery, et al.
European Journal of Human Genetics : EJHG|November 27, 2014
Genome-wide inbreeding estimation within Lebanese communities using SNP arraysNadine Jalkh, Mourad Sahbatou, Eliane Chouery, et al.
Human Reproduction (Oxford, England)|December 19, 2013
Does anonymous sperm donation increase the risk for unions between relatives and the incidence of autosomal recessive diseases due to consanguinity?Jean-Louis Serre, Anne-Louise Leutenegger, Alain Bernheim, et al.
Annals of Human Genetics|August 23, 2007
Familial Mediterranean Fever in Lebanon: founder effects for different MEFV mutationsNadine Jalkh, Emmanuelle Génin, Eliane Chouery, et al.
European Journal of Medical Genetics|August 28, 2007
Delayed transport of tissue-nonspecific alkaline phosphatase with missense mutations causing hypophosphatasiaIsabelle Brun-Heath, Anne-Sophie Lia-Baldini, Stéphane Maillard, et al.
Plos One|November 6, 2009
Involvement of the modifier gene of a human Mendelian disorder in a negative selection processIsabelle Jéru, Hasmik Hayrapetyan, Philippe Duquesnoy, et al.
BMC Medical Genetics|June 9, 2009
Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate allelesDelphine Fauvert, Isabelle Brun-Heath, Anne-Sophie Lia-Baldini, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Presse Medicale (Paris, France : 1983)|June 5, 2007
[Various topics in population genetics]Jean-Louis Serre
Molecular Genetics and Metabolism|February 8, 2005
Characterization of 11 novel mutations in the tissue non-specific alkaline phosphatase gene responsible for hypophosphatasia and genotype-phenotype correlationsIsabelle Brun-Heath, Agnes Taillandier, Jean-Louis Serre, et al.
Human Mutation|June 12, 2008
Mutations in TREM2 lead to pure early-onset dementia without bone cystsEliane Chouery, Valérie Delague, Anne Bergougnoux, et al.
European Journal of Human Genetics : EJHG|September 18, 2015
Genome-wide inbreeding estimation within Lebanese communities using SNP arraysNadine Jalkh, Mourad Sahbatou, Eliane Chouery, et al.
European Journal of Human Genetics : EJHG|November 27, 2014
Genome-wide inbreeding estimation within Lebanese communities using SNP arraysNadine Jalkh, Mourad Sahbatou, Eliane Chouery, et al.
Human Reproduction (Oxford, England)|December 19, 2013
Does anonymous sperm donation increase the risk for unions between relatives and the incidence of autosomal recessive diseases due to consanguinity?Jean-Louis Serre, Anne-Louise Leutenegger, Alain Bernheim, et al.
Annals of Human Genetics|August 23, 2007
Familial Mediterranean Fever in Lebanon: founder effects for different MEFV mutationsNadine Jalkh, Emmanuelle Génin, Eliane Chouery, et al.
European Journal of Medical Genetics|August 28, 2007
Delayed transport of tissue-nonspecific alkaline phosphatase with missense mutations causing hypophosphatasiaIsabelle Brun-Heath, Anne-Sophie Lia-Baldini, Stéphane Maillard, et al.
Plos One|November 6, 2009
Involvement of the modifier gene of a human Mendelian disorder in a negative selection processIsabelle Jéru, Hasmik Hayrapetyan, Philippe Duquesnoy, et al.
BMC Medical Genetics|June 9, 2009
Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate allelesDelphine Fauvert, Isabelle Brun-Heath, Anne-Sophie Lia-Baldini, et al.
Pageof 2