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E Mornet

Showing results (1-10 of 86) with videos related to

Pageof 9
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Human Mutation|March 29, 2000
Hypophosphatasia: the mutations in the tissue-nonspecific alkaline phosphatase geneE Mornet
Gynecologie, Obstetrique & Fertilite|November 19, 2003
[DNA, 50 years of the double helix: from the concept of molecular hybridization to microarrays]E Mornet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 7, 2018
Genetics of hypophosphatasiaE Mornet
Human Genetics|May 8, 2000
A 3D model of human P450c21: study of the putative effects of steroid 21-hydroxylase gene mutationsE Mornet, J F Gibrat
Gynecologie, Obstetrique & Fertilite|June 5, 2002
[Molecular genetic testing in amniotic fluid]B Simon-Bouy, E Mornet
Gynecologie, Obstetrique & Fertilite|June 29, 2010
[Non-invasive prenatal diagnosis: a tool for the future? Which consequences for our practices?]B Simon-Bouy, E Mornet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 12, 2004
[Genetics of hypophosphatasia]E Mornet, B Simon-Bouy
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1996
[Molecular biology of fragile X syndrome: recent data and diagnostic applications]E Mornet, B Simon-Bouy
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 12, 2004
[Childhood hypophosphatasia: a case report due to a novel mutation]C Draguet, Y Gillerot, E Mornet
Revue Francaise De Transfusion Et Immuno-Hematologie|February 1, 1985
[Strategies for the detection of DNA polymorphism in human populations]F Bastié-Sigeac, E Mornet, G Lucotte
Pageof 9

Showing results (1-10 of 86) with videos related to

Sort By:
Pageof 9
Human Mutation|March 29, 2000
Hypophosphatasia: the mutations in the tissue-nonspecific alkaline phosphatase geneE Mornet
Gynecologie, Obstetrique & Fertilite|November 19, 2003
[DNA, 50 years of the double helix: from the concept of molecular hybridization to microarrays]E Mornet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 7, 2018
Genetics of hypophosphatasiaE Mornet
Human Genetics|May 8, 2000
A 3D model of human P450c21: study of the putative effects of steroid 21-hydroxylase gene mutationsE Mornet, J F Gibrat
Gynecologie, Obstetrique & Fertilite|June 5, 2002
[Molecular genetic testing in amniotic fluid]B Simon-Bouy, E Mornet
Gynecologie, Obstetrique & Fertilite|June 29, 2010
[Non-invasive prenatal diagnosis: a tool for the future? Which consequences for our practices?]B Simon-Bouy, E Mornet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 12, 2004
[Genetics of hypophosphatasia]E Mornet, B Simon-Bouy
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1996
[Molecular biology of fragile X syndrome: recent data and diagnostic applications]E Mornet, B Simon-Bouy
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 12, 2004
[Childhood hypophosphatasia: a case report due to a novel mutation]C Draguet, Y Gillerot, E Mornet
Revue Francaise De Transfusion Et Immuno-Hematologie|February 1, 1985
[Strategies for the detection of DNA polymorphism in human populations]F Bastié-Sigeac, E Mornet, G Lucotte
Pageof 9