Françoise Denoyelle

Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

Françoise Denoyelle, Dominique Weil, Marion A. Maw et al. · Human Molecular Genetics · 1997 · 636 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann et al. · The American Journal of Human Genetics · 2005 · 559 citations · Full text

Medicine, Genetics, Otolaryngology +12

Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling

Françoise Denoyelle, Sandrine Marlin, Dominique Weil et al. · The Lancet · 1999 · 437 citations

Medicine, Genetics, Molecular Genetics +13

SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations

Sébastien Albert, Hélène Blons, Laurence Jonard et al. · European Journal of Human Genetics · 2006 · 243 citations

Medicine, Genetics, Molecular Genetics +12

Role of Propranolol in the therapeutic strategy of infantile laryngotracheal hemangioma

Françoise Denoyelle, Nicolas Leboulanger, O Enjolras et al. · International Journal of Pediatric Otorhinolaryngology · 2009 · 235 citations

Medicine, Otolaryngology, Pharmacology +11