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Showing results (631-640 of 642) with videos related to

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European Annals of Otorhinolaryngology, Head and Neck Diseases|September 1, 2020
The French Cochlear Implant Registry (EPIIC): Perception and language results in infants with cochlear implantation under the age of 24 monthsN Loundon, F Simon, K Aubry, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases|August 23, 2020
The French National Cochlear Implant Registry (EPIIC): Cochlear explantation and reimplantationR Hermann, A Coudert, K Aubry, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases|August 15, 2020
The French National Cochlear Implant Registry (EPIIC): Results, quality of life, questionnaires, academic and professional lifeF Artières-Sterkers, M Mondain, K Aubry, et al.
Journal of Medical Genetics|December 20, 2011
A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial featuresAnna-Maja Molin, J Andrieux, D A Koolen, et al.
Molecular Syndromology|November 4, 2010
IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS SignL Desmyter, M Ghassibe, N Revencu, et al.
Clinical Genetics|March 26, 2018
Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French casesS Baer, A Afenjar, T Smol, et al.
Human Mutation|November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndromeV Laugel, C Dalloz, M Durand, et al.
Clinical Genetics|November 20, 2015
Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national surveyM Lefebvre, D Sanlaville, N Marle, et al.
Reports on Progress in Physics. Physical Society (Great Britain)|May 6, 2022
Simple and statistically sound recommendations for analysing physical theoriesShehu S AbdusSalam, Fruzsina J Agocs, Benjamin C Allanach, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
Pageof 65

Showing results (631-640 of 642) with videos related to

Sort By:
Pageof 65
European Annals of Otorhinolaryngology, Head and Neck Diseases|September 1, 2020
The French Cochlear Implant Registry (EPIIC): Perception and language results in infants with cochlear implantation under the age of 24 monthsN Loundon, F Simon, K Aubry, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases|August 23, 2020
The French National Cochlear Implant Registry (EPIIC): Cochlear explantation and reimplantationR Hermann, A Coudert, K Aubry, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases|August 15, 2020
The French National Cochlear Implant Registry (EPIIC): Results, quality of life, questionnaires, academic and professional lifeF Artières-Sterkers, M Mondain, K Aubry, et al.
Journal of Medical Genetics|December 20, 2011
A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial featuresAnna-Maja Molin, J Andrieux, D A Koolen, et al.
Molecular Syndromology|November 4, 2010
IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS SignL Desmyter, M Ghassibe, N Revencu, et al.
Clinical Genetics|March 26, 2018
Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French casesS Baer, A Afenjar, T Smol, et al.
Human Mutation|November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndromeV Laugel, C Dalloz, M Durand, et al.
Clinical Genetics|November 20, 2015
Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national surveyM Lefebvre, D Sanlaville, N Marle, et al.
Reports on Progress in Physics. Physical Society (Great Britain)|May 6, 2022
Simple and statistically sound recommendations for analysing physical theoriesShehu S AbdusSalam, Fruzsina J Agocs, Benjamin C Allanach, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
Pageof 65