Delphine Feldmann

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

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

Ralf Birkenhäger, Edgar A. Otto, Maria J. Schürmann et al. · Nature Genetics · 2001 · 538 citations

Medicine, Nephrology, Neurology +9

Mutations in the Chloride Channel Gene CLCNKB as a Cause of Classic Bartter Syndrome

Martin Konrad, Martin Vollmer, Henny H. Lemmink et al. · Journal of the American Society of Nephrology · 2000 · 292 citations

Medicine, Genetics, Molecular Genetics +17

Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France

Mireille Claustres, Caroline Guittard, Dominique Bozon et al. · Human Mutation · 2000 · 250 citations

Life Sciences, Genetics, Molecular Genetics +11

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