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European Annals of Otorhinolaryngology, Head and Neck Diseases
|
August 9, 2020
The French Cochlear Implant Registry (EPIIC): Cochlear implant candidacy assessment of off-label indications
R Quatre, C Fabre, K Aubry, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
August 11, 2020
The French National Cochlear Implant Registry (EPIIC): Cochlear implantation in adults over 65years old
I Mosnier, E Ferrary, K Aubry, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
August 3, 2020
The French National Cochlear Implant Registry (EPIIC): Bilateral cochlear implantation
M Puechmaille, C Lambert, K Aubry, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
August 31, 2020
The French Cochlear Implant Registry (EPIIC): Cochlear implantation complications
V Parent, M Codet, K Aubry, et al.
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 months
N 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 reimplantation
R 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 life
F 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 features
Anna-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 Sign
L 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 cases
S Baer, A Afenjar, T Smol, et al.
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Search research articles
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Showing results (791-800 of 806) with videos related to
Sort By:
Page
of 81
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
August 9, 2020
The French Cochlear Implant Registry (EPIIC): Cochlear implant candidacy assessment of off-label indications
R Quatre, C Fabre, K Aubry, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
August 11, 2020
The French National Cochlear Implant Registry (EPIIC): Cochlear implantation in adults over 65years old
I Mosnier, E Ferrary, K Aubry, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
August 3, 2020
The French National Cochlear Implant Registry (EPIIC): Bilateral cochlear implantation
M Puechmaille, C Lambert, K Aubry, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
August 31, 2020
The French Cochlear Implant Registry (EPIIC): Cochlear implantation complications
V Parent, M Codet, K Aubry, et al.
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 months
N 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 reimplantation
R 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 life
F 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 features
Anna-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 Sign
L 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 cases
S Baer, A Afenjar, T Smol, et al.
Page
of 81