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	1.	DNA carrier detection in X-linked progressive cone dystrophy. [electronic resource] by Bergen, A A Meire, F Schuurman, E J Delleman, J W Producer: 19941004 In: Clinical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Nance-Horan syndrome: linkage analysis in a family from The Netherlands. [electronic resource] by Bergen, A A ten Brink, J Schuurman, E J Bleeker-Wagemakers, E M Producer: 19941019 In: Genomics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region. [electronic resource] by Bergen, A A ten Brink, J B Riemslag, F Schuurman, E J Tijmes, N Producer: 19950914 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Refinement of the localization of the X-linked ocular albinism gene. [electronic resource] by Bergen, A A Zijp, P Schuurman, E J Bleeker-Wagemakers, E M Apkarian, P van Ommen, G J Producer: 19930604 In: Genomics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3. [electronic resource] by Bergen, A A Meire, F ten Brink, J Schuurman, E J van Ommen, G J Delleman, J W Producer: 19940222 In: Genomics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Silent exonic mutations in the low-density lipoprotein receptor gene that cause familial hypercholesterolemia by affecting mRNA splicing. [electronic resource] by Defesche, J C Schuurman, E J M Klaaijsen, L N Khoo, K L Wiegman, A Stalenhoef, A F H Producer: 20080723 In: Clinical genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1. [electronic resource] by Bergen, A A ten Brink, J B Riemslag, F Schuurman, E J Meire, F Tijmes, N de Jong, P T Producer: 19970221 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey. [electronic resource] by van Langen, I M Birnie, E Schuurman, E Tan, H L Hofman, N Bonsel, G J Wilde, A A M Producer: 20051020 In: Clinical genetics vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa families. [electronic resource] by Bergen, A A Van den Born, L I Schuurman, E J Pinckers, A J Van Ommen, G J Bleekers-Wagemakers, E M Sandkuijl, L A Producer: 19960111 In: Ophthalmic genetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloning. [electronic resource] by Bergen, A A Wapenaar, M C Schuurman, E J Diergaarde, P J Lerach, H Monaco, A P Bakker, E Bleeker-Wagemakers, E M van Ommen, G J Producer: 19930330 In: Cytogenetics and cell genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type. [electronic resource] by Bergen, A A Samanns, C Schuurman, E J van Osch, L van Dorp, D B Pinckers, A J Bakker, E Gal, A van Ommen, G J Bleeker-Wagemakers, E M Producer: 19920204 In: Human genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Mutations in ABCC6 cause pseudoxanthoma elasticum. [electronic resource] by Bergen, A A Plomp, A S Schuurman, E J Terry, S Breuning, M Dauwerse, H Swart, J Kool, M van Soest, S Baas, F ten Brink, J B de Jong, P T Producer: 20000629 In: Nature genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysis. [electronic resource] by Bergen, A A Schuurman, E J van den Born, L I Samanns, C van Dorp, D B Pinckers, A J Bakker, E van Ommen, G J Gal, A Bleeker-Wagemakers, E M Producer: 19920521 In: Clinical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)