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	1.	Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome. [electronic resource] by Schrauwen, I Sommen, M Claes, C Pinner, J Flaherty, M Collins, F Van Camp, G Producer: 20150512 In: Clinical genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Correlation between laminin-5 immunohistochemistry and human papillomavirus status in squamous cervical carcinoma. [electronic resource] by Boulet, G A V Schrauwen, I Sahebali, S Horvath, C Depuydt, C E Vereecken, A Broeck, D Vanden Van Marck, E A Bogers, J J Producer: 20070910 In: Journal of clinical pathology vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	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)
	4.	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)
	5.	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)
	6.	A de novo splice site mutation in CASK causes FG syndrome-4 and congenital nystagmus. [electronic resource] by Dunn, P Prigatano, G P Szelinger, S Roth, J Siniard, A L Claasen, A M Richholt, R F De Both, M Corneveaux, J J Moskowitz, A M Balak, C Piras, I S Russell, M Courtright, A L Belnap, N Rangasamy, S Ramsey, K Opitz, J M Craig, D W Narayanan, V Huentelman, M J Schrauwen, I Producer: 20171019 In: American journal of medical genetics. Part A vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)