Cuny Bolder

Two Frequent Missense Mutations in Pendred Syndrome

Peter Van Hauwe, Lorraine A. Everett, Paul Coucke et al. · Human Molecular Genetics · 1998 · 192 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred’s syndrome

Cor W. R. J. Cremers, R.J.C. Admiraal, P.L.M. Huygen et al. · International Journal of Pediatric Otorhinolaryngology · 1998 · 88 citations

Medicine, Audiology, Otolaryngology +16

Progressive Sensorineural Hearing Loss and a Widened Vestibular Aqueduct in Pendred Syndrome

C. W. R. J. Cremers, Cuny Bolder, R.J.C. Admiraal et al. · Archives of Otolaryngology - Head and Neck Surgery · 1998 · 82 citations

Medicine, Endocrinology, Otolaryngology +17

The Gene for Pendred Syndrome Is Located between D7S501 and D7S692 in a 1.7-cM Region on Chromosome 7q

Paul Coucke, Guy Van Camp, Osman Demırhan et al. · Genomics · 1997 · 27 citations · Full text

Life Sciences, Genetics, Molecular Genetics +5