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Pierre Chauvin

Showing results (121-130 of 125) with videos related to

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Annals of the Rheumatic Diseases|August 7, 2023
Benralizumab for eosinophilic granulomatosis with polyangiitisAdrien Cottu, Matthieu Groh, Charlene Desaintjean, et al.
Antimicrobial Agents and Chemotherapy|April 28, 2005
Virological and pharmacological parameters predicting the response to lopinavir-ritonavir in heavily protease inhibitor-experienced patientsAnne-Geneviève Marcelin, Isabelle Cohen-Codar, Martin S King, et al.
European Journal of Human Genetics : EJHG|March 30, 2006
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populationsSébastien Albert, Hélène Blons, Laurence Jonard, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: genotypic and phenotypic analysisDelphine Feldmann, Françoise Denoyelle, Pierre Chauvin, et al.
Archives of Otolaryngology--Head & Neck Surgery|June 22, 2005
GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patientsSandrine Marlin, Delphine Feldmann, Hélène Blons, et al.
Pageof 13

Showing results (121-130 of 125) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 125 results.
Annals of the Rheumatic Diseases|August 7, 2023
Benralizumab for eosinophilic granulomatosis with polyangiitisAdrien Cottu, Matthieu Groh, Charlene Desaintjean, et al.
Antimicrobial Agents and Chemotherapy|April 28, 2005
Virological and pharmacological parameters predicting the response to lopinavir-ritonavir in heavily protease inhibitor-experienced patientsAnne-Geneviève Marcelin, Isabelle Cohen-Codar, Martin S King, et al.
European Journal of Human Genetics : EJHG|March 30, 2006
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populationsSébastien Albert, Hélène Blons, Laurence Jonard, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: genotypic and phenotypic analysisDelphine Feldmann, Françoise Denoyelle, Pierre Chauvin, et al.
Archives of Otolaryngology--Head & Neck Surgery|June 22, 2005
GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patientsSandrine Marlin, Delphine Feldmann, Hélène Blons, et al.
Pageof 13