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C Petit

Showing results (321-330 of 563) with videos related to

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Human Mutation|January 4, 2001
Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysisI Zwaenepoel, E Verpy, S Blanchard, et al.
Mechanisms of Development|December 10, 1999
Characterization of the two zebrafish orthologues of the KAL-1 gene underlying X chromosome-linked Kallmann syndromeO Ardouin, R Legouis, L Fasano, et al.
International Archives of Allergy and Immunology|October 1, 1994
Modulation of IgE production in the mouse by beta 2-adrenoceptor agonistO Coqueret, C Petit-Frère, V Lagente, et al.
Archives De L'Institut Pasteur De Tunis|January 1, 1997
Contribution of DFNB1 and DFNB2 loci to neurosensory deafness in affected Tunisian familiesA Boulila-Elgaïed, S Masmoudi, M Drira, et al.
Applied Physics Letters|July 30, 2015
Highly tunable perpendicularly magnetized synthetic antiferromagnets for biotechnology applicationsT Vemulkar, R Mansell, D C M C Petit, et al.
Archives of Gynecology and Obstetrics|November 25, 2019
Is homecare management associated with longer latency in preterm premature rupture of membranes?M Guckert, E Clouqueur, E Drumez, et al.
Applied Physics Letters|February 14, 2017
The mechanical response in a fluid of synthetic antiferromagnetic and ferrimagnetic microdiscs with perpendicular magnetic anisotropyT Vemulkar, E N Welbourne, R Mansell, et al.
Lancet (London, England)|April 28, 1999
Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counsellingF Denoyelle, S Marlin, D Weil, et al.
Human Molecular Genetics|December 1, 1994
A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene intervalH Chaïb, G Lina-Granade, P Guilford, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|May 27, 1982
[Relationship with height- and weight-characteristics]Y Spyckerelle, J P Deschamps, J L André, et al.
Pageof 57

Showing results (321-330 of 563) with videos related to

Sort By:
Pageof 57
Human Mutation|January 4, 2001
Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysisI Zwaenepoel, E Verpy, S Blanchard, et al.
Mechanisms of Development|December 10, 1999
Characterization of the two zebrafish orthologues of the KAL-1 gene underlying X chromosome-linked Kallmann syndromeO Ardouin, R Legouis, L Fasano, et al.
International Archives of Allergy and Immunology|October 1, 1994
Modulation of IgE production in the mouse by beta 2-adrenoceptor agonistO Coqueret, C Petit-Frère, V Lagente, et al.
Archives De L'Institut Pasteur De Tunis|January 1, 1997
Contribution of DFNB1 and DFNB2 loci to neurosensory deafness in affected Tunisian familiesA Boulila-Elgaïed, S Masmoudi, M Drira, et al.
Applied Physics Letters|July 30, 2015
Highly tunable perpendicularly magnetized synthetic antiferromagnets for biotechnology applicationsT Vemulkar, R Mansell, D C M C Petit, et al.
Archives of Gynecology and Obstetrics|November 25, 2019
Is homecare management associated with longer latency in preterm premature rupture of membranes?M Guckert, E Clouqueur, E Drumez, et al.
Applied Physics Letters|February 14, 2017
The mechanical response in a fluid of synthetic antiferromagnetic and ferrimagnetic microdiscs with perpendicular magnetic anisotropyT Vemulkar, E N Welbourne, R Mansell, et al.
Lancet (London, England)|April 28, 1999
Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counsellingF Denoyelle, S Marlin, D Weil, et al.
Human Molecular Genetics|December 1, 1994
A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene intervalH Chaïb, G Lina-Granade, P Guilford, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|May 27, 1982
[Relationship with height- and weight-characteristics]Y Spyckerelle, J P Deschamps, J L André, et al.
Pageof 57