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L Moatti

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Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris|January 1, 1990
[Development of tone curves in sensorineural deafness in children]L Moatti, E N Garabedian, H Lacombe, et al.
Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris|January 1, 1994
[Audiophonologic aspects of the decision and follow-up of cochlear implants in children]L Moatti, E N Garabedian, D Magnier, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 5, 2002
Hypogonadotrophic hypogonadism associated with prelingual deafness due to a connexin 26 gene mutationM Houang, M Gourmelen, L Moatti, et al.
Lancet (London, England)|April 28, 1999
Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counsellingF Denoyelle, S Marlin, D Weil, et al.
Neuroepidemiology|January 1, 1987
Studies on an isolated West Indies population. III. Epidemiologic study of sensorineural hearing lossE Bois, C Bonaïti, M Lallemant, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 5, 2001
Connexin 26 gene mutations in congenitally deaf children: pitfalls for genetic counselingS Marlin, E N Garabédian, G Roger, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

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Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris|January 1, 1990
[Development of tone curves in sensorineural deafness in children]L Moatti, E N Garabedian, H Lacombe, et al.
Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris|January 1, 1994
[Audiophonologic aspects of the decision and follow-up of cochlear implants in children]L Moatti, E N Garabedian, D Magnier, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 5, 2002
Hypogonadotrophic hypogonadism associated with prelingual deafness due to a connexin 26 gene mutationM Houang, M Gourmelen, L Moatti, et al.
Lancet (London, England)|April 28, 1999
Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counsellingF Denoyelle, S Marlin, D Weil, et al.
Neuroepidemiology|January 1, 1987
Studies on an isolated West Indies population. III. Epidemiologic study of sensorineural hearing lossE Bois, C Bonaïti, M Lallemant, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 5, 2001
Connexin 26 gene mutations in congenitally deaf children: pitfalls for genetic counselingS Marlin, E N Garabédian, G Roger, et al.
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