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	1.	[From gene to disease: deafness and connexin 26]. [electronic resource] by Hoefsloot, L H Kemperman, M Cremers, C W R J Producer: 20020613 In: Nederlands tijdschrift voor geneeskunde vol. 146 Availability: No items available. Save to lists Add to cart (remove)
	2.	Progressive fluctuant hearing loss, enlarged vestibular aqueduct, and cochlear hypoplasia in branchio-oto-renal syndrome. [electronic resource] by Kemperman, M H Stinckens, C Kumar, S Huygen, P L Joosten, F B Cremers, C W Producer: 20011207 In: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	The branchio-oto-renal syndrome. [electronic resource] by Kemperman, M H Stinckens, C Kumar, S Joosten, F B M Huygen, P L M Cremers, C W R J Producer: 20030226 In: Advances in oto-rhino-laryngology vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Underreporting of Lyme and Other Tick-Borne Diseases in Residents of a High-Incidence County, Minnesota, 2009. [electronic resource] by Schiffman, E K McLaughlin, C Ray, J A E Kemperman, M M Hinckley, A F Friedlander, H G Neitzel, D F Producer: 20180530 In: Zoonoses and public health vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9. [electronic resource] by Bom, S J Kemperman, M H De Kok, Y J Huygen, P L Verhagen, W I Cremers, F P Cremers, C W Producer: 19991014 In: The Laryngoscope vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	[From gene to disease; a progressive cochlear-vestibular dysfunction with onset in middle-age (DFNA9)]. [electronic resource] by Cremers, C W R Kemperman, M H Bom, S J H Huygen, P L M Verhagen, W I M Kremer, J M J Producer: 20060110 In: Nederlands tijdschrift voor geneeskunde vol. 149 Availability: No items available. Save to lists Add to cart (remove)
	7.	A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26). [electronic resource] by van Wijk, E Krieger, E Kemperman, M H De Leenheer, E M R Huygen, P L M Cremers, C W R J Cremers, F P M Kremer, H Producer: 20040223 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH. [electronic resource] by Bom, S J De Leenheer, E M Lemaire, F X Kemperman, M H Verhagen, W I Marres, H A Kunst, H P Ensink, R J Bosman, A J Van Camp, G Cremers, F P Huygen, P L Cremers, C W Producer: 20011025 In: Archives of otolaryngology--head & neck surgery vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects. [electronic resource] by de Kok, Y J Bom, S J Brunt, T M Kemperman, M H van Beusekom, E van der Velde-Visser, S D Robertson, N G Morton, C C Huygen, P L Verhagen, W I Brunner, H G Cremers, C W Cremers, F P Producer: 19990318 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation. [electronic resource] by Fransen, E Verstreken, M Bom, S J Lemaire, F Kemperman, M H De Kok, Y J Wuyts, F L Verhagen, W I Huygen, P L McGuirt, W T Smith, R J Van Maldergem, L V Declau, F Cremers, C W Van De Heyning, P H Cremers, F P Van Camp, G Producer: 20010510 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)