D. V. van Dorp

发表

A decisive electrophysiological test for human albinism.

H Spekreijse, D Reits, P Apkarian, 1983, Electroencephalography and clinical neurophysiology.

Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibship.

P. Barth, D. V. van Dorp, M. Kwee, 1991, American journal of medical genetics.

The Hermansky-Pudlak syndrome. Variable reaction to 1-desamino-8D-arginine vasopressin for correction of the bleeding time.

G. Vrensen, F. Meire, P. Wijermans, 1990, Ophthalmic paediatrics and genetics.

Hermansky‐pudlak syndrome: Correction of bleeding time by 1‐desamino‐8D‐arginine vasopressin

P. Wijermans, D. V. van Dorp, P. Wijermans, 1989, American journal of hematology.

Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis.

A. Bergen, A. Gal, C. Samanns, 1990, Ophthalmic paediatrics and genetics.

Albinism, or the NOACH syndrome (the book of Enoch c.v. 1-20).

D. V. van Dorp, 1987, Clinical genetics.

A family with X-chromosomal recessive congenital cataract, microphthalmia, a peculiar form of the ear and dental anomalies.

D. V. van Dorp, J. Delleman, 1979, Journal of pediatric ophthalmology and strabismus.

Linkage analysis in X-linked congenital stationary night blindness.

K. Dry, M. Jay, P. Teague, 1992, Genomics.

Tuberous sclerosis. Diagnostic problems in a family.

D. V. van Dorp, M. Kwee, 1990, Ophthalmic Paediatrics and Genetics.

Kabuki syndrome – Report of six cases and review of the literature with emphasis on ocular features

M. Warburg, A. Toutain, I. Kluijt, 2000, Ophthalmic genetics.

Identification of a 5′ splice site mutation in the RPGR gene in a family with X‐linked retinitis pigmentosa (RP3)

K. Dry, A. Lennon, A. Wright, 1999, Human mutation.

X-linked congenital stationary night blindness: review and report of a family with hyperopia.

D. V. van Dorp, A. Wright, 1991, A M A Archives of Ophthalmology.