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Clinical Otolaryngology and Allied Sciences|June 1, 1992
Hearing with the bone-anchored hearing aid (BAHA, HC 200) compared to a conventional bone-conduction hearing aidC W Cremers, F M Snik, A J BeynonInternational Journal of Pediatric Otorhinolaryngology|September 1, 1989
Hearing levels in the Cornelia de Lange syndrome. A report of seven casesH A Marres, C W Cremers, P H JongbloetAnnals of the New York Academy of Sciences|January 1, 1991
Nonsyndromal profound genetic deafness in childhoodC W Cremers, H A Marres, P M van RijnInternational Journal of Pediatric Otorhinolaryngology|August 1, 1994
The sex-ratio in childhood deafness, an analysis of the male predominanceC W Cremers, P M van Rijn, P L HuygenAmerican Journal of Medical Genetics|April 29, 1998
Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13S Kumar, H A Marres, C W Cremers, et al.Clinical Genetics|November 1, 1975
The Nathalie syndrome. A new hereditary syndromeC W Cremers, B G Ter Haar, T J Van RensClinical Otolaryngology and Allied Sciences|June 29, 1999
The BAHA HC200/300 in comparison with conventional bone conduction hearing aidsC T van der Pouw, A F Snik, C W CremersThe Annals of Otology, Rhinology, and Laryngology|June 23, 1999
Percutaneous implants in the temporal bone for securing a bone conductor: surgical methods and resultsC T van der Pouw, E A Mylanus, C W CremersThe Laryngoscope|April 18, 1998
Audiometric results of bilateral bone-anchored hearing aid application in patients with bilateral congenital aural atresiaK T van der Pouw, A F Snik, C W CremersThe American Journal of Otology|November 1, 1996
Carriers of the Usher syndrome type IB: is audiometric identification possible?M Wagenaar, A F Snik, W J Kimberling, et al.Pageof 16