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 · 635 citations · Full text

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 · 551 citations · Full text

Genetic Disorder, Genetics, Audiology +9

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

Developmental Anomaly, Mendelian Disorder, Genetic Disorder +10

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 · 240 citations · Full text

Developmental Biology, Medicine, Genetics +11

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

Pharmacology, Infantile Laryngotracheal Hemangioma, Therapeutic Strategy