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European Annals of Otorhinolaryngology, Head and Neck Diseases|December 16, 2022
Recurrent benign paroxysmal positional vertigo in two DFNB16 siblings: A CARE case reportS Achard, F Simon, F Denoyelle, et al.European Annals of Otorhinolaryngology, Head and Neck Diseases|September 5, 2020
Myringoplasty without tympanomeatal flap elevation in children: A systematic reviewF Chatelet, N Leboulanger, S Achard, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 10, 2012
[Genetic aspects of congenital sensorineural hearing loss]M Blanchard, B Thierry, S Marlin, et al.La Revue Du Praticien|March 29, 2000
[Hereditary sensorineural deafness]F Denoyelle, S Marlin, C Petit, et al.Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris|October 10, 1998
[Etiological diagnosis of sensorineural deafness in children: a year-long review of genetic counseling for deaf people]S Marlin, F Denoyelle, E N Garabédian, et al.International Journal of Pediatric Otorhinolaryngology|August 28, 1998
A particular case of deafness-oligodontia syndromeS Marlin, F Denoyelle, D Busquet, et al.The Journal of Laryngology and Otology|November 25, 2021
Shedding light on the tympanic membrane: a brief history of the description and understanding of its anatomyR Baudouin, F Denoyelle, F SimonLancet (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.European Annals of Otorhinolaryngology, Head and Neck Diseases|August 17, 2020
Lateral endoscopic parathyroidectomy in childrenR Baudouin, F Simon, F Denoyelle, 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 79