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Jean-Pierre Hardelin

Showing results (1-10 of 66) with videos related to

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Medecine Sciences : M/S|September 7, 2021
[Foreword: Chronic diseases: Transition between adolescence to adulthood]Jean-Pierre Hardelin
Medecine Sciences : M/S|September 14, 2004
[Kallmann De Morsier syndrome: FGF-signaling insufficiency?]Catherine Dodé, Jean-Pierre Hardelin
Medecine Sciences : M/S|January 7, 2020
[Congenital deafness forms: progressing toward gene therapy?]Jean-Pierre Hardelin, Saaid Safieddine
Journal of Molecular Medicine (Berlin, Germany)|September 15, 2004
Kallmann syndrome: fibroblast growth factor signaling insufficiency?Catherine Dodé, Jean-Pierre Hardelin
European Journal of Human Genetics : EJHG|November 6, 2008
Kallmann syndromeCatherine Dodé, Jean-Pierre Hardelin
The New England Journal of Medicine|August 15, 2003
Molecular mechanism of a frequent genetic form of deafnessVincent Michel, Jean-Pierre Hardelin, Christine Petit
Medecine Sciences : M/S|August 24, 2005
[Usher syndrome type I and the differentiation of inner ear sensory cells' hair bundles]Aziz El-Amraoui, Gaëlle Lefèvre, Jean-Pierre Hardelin, et al.
Medecine Sciences : M/S|March 9, 2011
[Kallmann syndrome - a fetopathological sequence]Fabien Guimiot, Luis Teixeira, Catherine Dodé, et al.
Medecine Sciences : M/S|April 7, 2004
[Hereditary deafness: molecular genetics]Jean-Pierre Hardelin, Françoise Denoyelle, Jacqueline Levilliers, et al.
European Journal of Endocrinology|September 14, 2013
Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patientsJulie Sarfati, Corinne Fouveaut, Chrystel Leroy, et al.
Pageof 7

Showing results (1-10 of 66) with videos related to

Sort By:
Pageof 7
Medecine Sciences : M/S|September 7, 2021
[Foreword: Chronic diseases: Transition between adolescence to adulthood]Jean-Pierre Hardelin
Medecine Sciences : M/S|September 14, 2004
[Kallmann De Morsier syndrome: FGF-signaling insufficiency?]Catherine Dodé, Jean-Pierre Hardelin
Medecine Sciences : M/S|January 7, 2020
[Congenital deafness forms: progressing toward gene therapy?]Jean-Pierre Hardelin, Saaid Safieddine
Journal of Molecular Medicine (Berlin, Germany)|September 15, 2004
Kallmann syndrome: fibroblast growth factor signaling insufficiency?Catherine Dodé, Jean-Pierre Hardelin
European Journal of Human Genetics : EJHG|November 6, 2008
Kallmann syndromeCatherine Dodé, Jean-Pierre Hardelin
The New England Journal of Medicine|August 15, 2003
Molecular mechanism of a frequent genetic form of deafnessVincent Michel, Jean-Pierre Hardelin, Christine Petit
Medecine Sciences : M/S|August 24, 2005
[Usher syndrome type I and the differentiation of inner ear sensory cells' hair bundles]Aziz El-Amraoui, Gaëlle Lefèvre, Jean-Pierre Hardelin, et al.
Medecine Sciences : M/S|March 9, 2011
[Kallmann syndrome - a fetopathological sequence]Fabien Guimiot, Luis Teixeira, Catherine Dodé, et al.
Medecine Sciences : M/S|April 7, 2004
[Hereditary deafness: molecular genetics]Jean-Pierre Hardelin, Françoise Denoyelle, Jacqueline Levilliers, et al.
European Journal of Endocrinology|September 14, 2013
Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patientsJulie Sarfati, Corinne Fouveaut, Chrystel Leroy, et al.
Pageof 7