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Dominique Weil

Showing results (41-50 of 84) with videos related to

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Neurogenetics|April 11, 2003
Gene structure, chromosomal localization, and mutation screening of the human gene for the inner ear protein otospiralinMireille Lavigne-Rebillard, Benjamin Delprat, Marie-Odile Surget, et al.
Journal of Pediatric Surgery|October 23, 2015
Laparoscopic adjustable gastric banding in adolescents: Results at two years including psychosocial aspectsFrançoise Schmitt, Elise Riquin, Marion Beaumesnil, et al.
Developmental Biology|May 11, 2005
Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cellsVincent Michel, Richard J Goodyear, Dominique Weil, et al.
Human Mutation|April 21, 2005
Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non-syndromic recessive hearing lossAbdelaziz Tlili, Ilhem Charfedine, Imed Lahmar, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34Mirna Mustapha, Eliane Chouery, Sébastien Chardenoux, et al.
Human Molecular Genetics|December 14, 2004
Interactions in the network of Usher syndrome type 1 proteinsAvital Adato, Vincent Michel, Yoshiaki Kikkawa, et al.
Journal of Laparoendoscopic & Advanced Surgical Techniques. Part A|November 1, 2008
Minimally invasive surgery for anorectal malformation in boys: a multicenter studyGuillaume Podevin, Thierry Petit, Pierre Yves Mure, et al.
Cell Reports|August 3, 2017
Dual RNA Processing Roles of Pat1b via Cytoplasmic Lsm1-7 and Nuclear Lsm2-8 ComplexesCaroline Vindry, Aline Marnef, Helen Broomhead, et al.
Nucleic Acids Research|June 26, 2016
The DDX6-4E-T interaction mediates translational repression and P-body assemblyAnastasiia Kamenska, Clare Simpson, Caroline Vindry, et al.
Molecular Genetics & Genomic Medicine|June 2, 2015
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencingFatima Ammar-Khodja, Crystel Bonnet, Malika Dahmani, et al.
Pageof 9

Showing results (41-50 of 84) with videos related to

Sort By:
Pageof 9
Neurogenetics|April 11, 2003
Gene structure, chromosomal localization, and mutation screening of the human gene for the inner ear protein otospiralinMireille Lavigne-Rebillard, Benjamin Delprat, Marie-Odile Surget, et al.
Journal of Pediatric Surgery|October 23, 2015
Laparoscopic adjustable gastric banding in adolescents: Results at two years including psychosocial aspectsFrançoise Schmitt, Elise Riquin, Marion Beaumesnil, et al.
Developmental Biology|May 11, 2005
Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cellsVincent Michel, Richard J Goodyear, Dominique Weil, et al.
Human Mutation|April 21, 2005
Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non-syndromic recessive hearing lossAbdelaziz Tlili, Ilhem Charfedine, Imed Lahmar, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34Mirna Mustapha, Eliane Chouery, Sébastien Chardenoux, et al.
Human Molecular Genetics|December 14, 2004
Interactions in the network of Usher syndrome type 1 proteinsAvital Adato, Vincent Michel, Yoshiaki Kikkawa, et al.
Journal of Laparoendoscopic & Advanced Surgical Techniques. Part A|November 1, 2008
Minimally invasive surgery for anorectal malformation in boys: a multicenter studyGuillaume Podevin, Thierry Petit, Pierre Yves Mure, et al.
Cell Reports|August 3, 2017
Dual RNA Processing Roles of Pat1b via Cytoplasmic Lsm1-7 and Nuclear Lsm2-8 ComplexesCaroline Vindry, Aline Marnef, Helen Broomhead, et al.
Nucleic Acids Research|June 26, 2016
The DDX6-4E-T interaction mediates translational repression and P-body assemblyAnastasiia Kamenska, Clare Simpson, Caroline Vindry, et al.
Molecular Genetics & Genomic Medicine|June 2, 2015
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencingFatima Ammar-Khodja, Crystel Bonnet, Malika Dahmani, et al.
Pageof 9