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Clinical Genetics|May 1, 1993
Linkage analysis in a family with complete type congenital stationary night blindness with and without myopiaK L Dry, D B Van Dorp, M A Aldred, et al.Ophthalmic Genetics|April 26, 2000
Kabuki syndrome - report of six cases and review of the literature with emphasis on ocular featuresI Kluijt, D B van Dorp, M L Kwee, et al.Ophthalmic Paediatrics and Genetics|September 1, 1990
Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysisA A Bergen, C Samanns, D B Van Dorp, et al.Clinical Genetics|December 1, 1985
Aland eye disease: no albino misroutingD B van Dorp, A W Eriksson, J W Delleman, et al.Genomics|September 1, 1992
Linkage analysis in X-linked congenital stationary night blindnessM A Aldred, K L Dry, D M Sharp, et al.Human Genetics|December 1, 1991
Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls typeA A Bergen, C Samanns, E J Schuurman, et al.Clinical Genetics|March 1, 1992
Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysisA A Bergen, E J Schuurman, L I van den Born, et al.Pageof 3