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	61.	Hirschsprung disease and L1CAM: is the disturbed sex ratio caused by L1CAM mutations? [electronic resource] by Hofstra, R M W Elfferich, P Osinga, J Verlind, E Fransen, E López Pisón, J de Die-Smulders, C E M Stolte-Dijkstra, I Buys, C H C M Producer: 20020729 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Involvement of T-cell receptor-beta alterations in the development of otosclerosis linked to OTSC2. [electronic resource] by Schrauwen, I Venken, K Vanderstraeten, K Thys, M Hendrickx, J-J Fransen, E Van Laer, L Govaerts, P J Verstreken, M Schatteman, I Stinissen, P Hellings, N Van Camp, G Producer: 20100820 In: Genes and immunity vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	A new locus for otosclerosis, OTSC10, maps to chromosome 1q41-44. [electronic resource] by Schrauwen, I Weegerink, N J D Fransen, E Claes, C Pennings, R J E Cremers, C W R J Huygen, P L M Kunst, H P M Van Camp, G Producer: 20110802 In: Clinical genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patients. [electronic resource] by Thys, M Schrauwen, I Vanderstraeten, K Dieltjens, N Fransen, E Ealy, M Cremers, C W R J van de Heyning, P Vincent, R Offeciers, E Smith, R H van Camp, G Producer: 20090318 In: Annals of human genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	Candidate gene association study for noise-induced hearing loss in two independent noise-exposed populations. [electronic resource] by Konings, A Van Laer, L Wiktorek-Smagur, A Rajkowska, E Pawelczyk, M Carlsson, P I Bondeson, M L Dudarewicz, A Vandevelde, A Fransen, E Huyghe, J Borg, E Sliwinska-Kowalska, M Van Camp, G Producer: 20090318 In: Annals of human genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH gene. [electronic resource] by Verstreken, M Declau, F Wuyts, F L D'Haese, P Van Camp, G Fransen, E Van den Hauwe, L Buyle, S Smets, R E Feenstra, L Van der Stappen, A Van de Heyning, P H Producer: 20020208 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)
	67.	Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European population. [electronic resource] by Bonneux, S Fransen, E Van Eyken, E Van Laer, L Huyghe, J Van de Heyning, P Voets, A Gerards, M Stassen, A P M Hendrickx, A T M Smeets, H J M Van Camp, G Producer: 20111201 In: Mitochondrion vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene. [electronic resource] by Fransen, E Verstreken, M Verhagen, W I Wuyts, F L Huygen, P L D'Haese, P Robertson, N G Morton, C C McGuirt, W T Smith, R J Declau, F Van de Heyning, P H Van Camp, G Producer: 19990914 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment. [electronic resource] by Van Laer, L Coucke, P Mueller, R F Caethoven, G Flothmann, K Prasad, S D Chamberlin, G P Houseman, M Taylor, G R Van de Heyning, C M Fransen, E Rowland, J Cucci, R A Smith, R J Van Camp, G Producer: 20011205 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)
	70.	L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patterns. [electronic resource] by Fransen, E D'Hooge, R Van Camp, G Verhoye, M Sijbers, J Reyniers, E Soriano, P Kamiguchi, H Willemsen, R Koekkoek, S K De Zeeuw, C I De Deyn, P P Van der Linden, A Lemmon, V Kooy, R F Willems, P J Producer: 19980619 In: Human molecular genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	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)
	72.	Positional cloning of a gene involved in hereditary multiple exostoses. [electronic resource] by Wuyts, W Van Hul, W Wauters, J Nemtsova, M Reyniers, E Van Hul, E V De Boulle, K de Vries, B B Hendrickx, J Herrygers, I Bossuyt, P Balemans, W Fransen, E Vits, L Coucke, P Nowak, N J Shows, T B Mallet, L van den Ouweland, A M McGaughran, J Halley, D J Willems, P J Producer: 19970204 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment. [electronic resource] by Van Eyken, E Van Camp, G Fransen, E Topsakal, V Hendrickx, J J Demeester, K Van de Heyning, P Mäki-Torkko, E Hannula, S Sorri, M Jensen, M Parving, A Bille, M Baur, M Pfister, M Bonaconsa, A Mazzoli, M Orzan, E Espeso, A Stephens, D Verbruggen, K Huyghe, J Dhooge, I Huygen, P Kremer, H Cremers, C W R J Kunst, S Manninen, M Pyykkö, I Lacava, A Steffens, M Wienker, T F Van Laer, L Producer: 20071009 In: Journal of medical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	Familial aggregation of tinnitus: a European multicentre study. [electronic resource] by Hendrickx, J J Huyghe, J R Demeester, K Topsakal, V Van Eyken, E Fransen, E Mäki-Torkko, E Hannula, S Jensen, M Tropitzsch, A Bonaconsa, A Mazzoli, M Espeso, A Verbruggen, K Huyghe, J Huygen, P L M Kremer, H Kunst, S J Manninen, M Diaz-Lacava, A N Steffens, M Parving, A Pyykkö, I Dhooge, I Stephens, D Orzan, E Pfister, M H F Bille, M Sorri, M Cremers, C W R J Van Laer, L Van Camp, G Wienker, T F Van de Heyning, P Producer: 20080304 In: B-ENT vol. 3 Suppl 7 Availability: No items available. Save to lists Add to cart (remove)