Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type von BERGEN, A. A. B, SAMANNS, C, SCHUURMAN, E. J. M, VAN OSCH, L, VAN DORP, D. B, PINCKERS, A. J. L. G, BAKKER, E, GAL, A, VAN OMMEN, G. J. B, BLEEKER-WAGEMAKERS, E. M

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Linkage analysis in X-linked congenital stationary night blindness von Aldred, M.A., Dry, K.L., Sharp, D.M., Van Dorp, D.B., Brown, J., Hardwick, L.J., Lester, D.H., Pryde, F.E., Teague, P.W., Jay, M., Bird, A.C., Jay, B., Wright, A.F.

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A family with RP3 type of X-linked retinitis pigmentosa : an association with ciliary abnormalities von VAN DORP, D. B, WRIGHT, A. F, CAROTHERS, A. D, BLEEKER-WAGEMAKERS, E. M

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Hermansky‐pudlak syndrome: Correction of bleeding time by 1‐desamino‐8D‐arginine vasopressin von Wijermans, P. W., van Dorp, D. B.

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Albinism: phenotype or genotype? von VAN DORP, D. B, VAN HAERINGEN, N. J, DELLEMAN, J. W, APKARIAN, P, WESTERHOF, W

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Albinotic Characteristics in Congenital Nystagmus von Dorp, D. B. van

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Chopart Joint Injury: A Study of Outcome and Morbidity von van Dorp, Karin B., MD, de Vries, Mark R., MD, PhD, van der Elst, Maarten, MD, PhD, Schepers, Tim, MD, PhD

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Joubert syndrome: A clinical and pathological description of an affected male and a female fetus from the same sibship von van Dorp, Dieuwke B., Palan, Alzbeta, Kwee, Mei Lan, Barth, Peter G., van der Harten, Johan J.

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Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis von Bergen, A. A. B., Samanns, C., Van Dorp, D. B., Ferguson-Smith, M. A., Gal, A., Bleeker-Wagemakers, E. M.

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Identification of a 5′ splice site mutation in the RPGR gene in a family with X-linked retinitis pigmentosa (RP3) von Dry, Katherine L., Manson, Forbes D.C., Lennon, Alan, Bergen, Arthur A.B., Van Dorp, Dieuwke B., Wright, Alan F.

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The Hermansky-Pudlak syndrome: Variable reaction to 1-desamino-8D-arginine vasopressin for correction of the bleeding time von Van Dorp, D. B., Wijermans, P. W., Meire, F., Vrensen, G.

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Kabuki syndrome ? Report of six cases and review of the literature with emphasis on ocular features von Kluijt, I., van Dorp, D.B., Kwee, M.L., Toutain, A., Keppler-Noreuil, K., Warburg, M., Bitoun, P.

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Tuberous sclerosis Diagnostic problems in a family von Van Dorp, D. B., Kwee, M. L.

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Fluorescein angiography in potential carriers for choroideremia An additional aid for final diagnosis, when funduscopy shows equivocal symptoms von Van Dorp, D. B., Van Balen, A. Th. M.

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Kabuki syndrome - Report of six cases and review of the literature with emphasis on ocular features von Kluijt, I., van Dorp, D.B., Kwee, M.L., Toutain, A., Keppler-Noreuil, K., Warburg, M., Bitoun, P.

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Reply von van Dorp, D. B.

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Hornhauttrübung von van Pampus, E. C. M., Schouten, J. A., van Dorp, D. B., Mulder, C., Beynen, A. C.

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Reply von van Dorp, D. B.

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Reply von van Dorp, D. B.

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Corneal opacity von van Pampus, E C, Schouten, J A, van Dorp, D B, Mulder, C, Beynen, A C

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