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D B van Dorp

Showing results (11-20 of 21) with videos related to

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Documenta Ophthalmologica. Advances in Ophthalmology|December 15, 1983
Albinism: phenotype or genotype?D B van Dorp, N J van Haeringen, J W Delleman, et al.
Klinische Monatsblatter Fur Augenheilkunde|September 1, 1985
[Corneal opacity]E C van Pampus, J A Schouten, D B van Dorp, et al.
American Journal of Medical Genetics|July 1, 1991
Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibshipD B van Dorp, A Palan, M L Kwee, et al.
Human Mutation|March 27, 1999
Identification of a 5' splice site mutation in the RPGR gene in a family with X-linked retinitis pigmentosa (RP3)K L Dry, F D Manson, A Lennon, et al.
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.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Documenta Ophthalmologica. Advances in Ophthalmology|December 15, 1983
Albinism: phenotype or genotype?D B van Dorp, N J van Haeringen, J W Delleman, et al.
Klinische Monatsblatter Fur Augenheilkunde|September 1, 1985
[Corneal opacity]E C van Pampus, J A Schouten, D B van Dorp, et al.
American Journal of Medical Genetics|July 1, 1991
Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibshipD B van Dorp, A Palan, M L Kwee, et al.
Human Mutation|March 27, 1999
Identification of a 5' splice site mutation in the RPGR gene in a family with X-linked retinitis pigmentosa (RP3)K L Dry, F D Manson, A Lennon, et al.
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.
Pageof 3