D. B. van Dorp
Visio(NL)
Publications by Year
Research Areas
melanin and skin pigmentation, Retinal Development and Disorders, Retinoids in leukemia and cellular processes, Glaucoma and retinal disorders, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Most-Cited Works
- → A family with RP3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalities(1992)86 cited
- → Hermansky‐pudlak syndrome: Correction of bleeding time by 1‐desamino‐8D‐arginine vasopressin(1989)44 cited
- → Åland eye disease: no albino misrouting(1985)41 cited
- → Identification of a 5? splice site mutation in theRPGR gene in a family with X-linked retinitis pigmentosa (RP3)(1999)40 cited
- → Joubert syndrome: A clinical and pathological description of an affected male and a female fetus from the same sibship(1991)38 cited
- → Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type(1991)35 cited
- → Kabuki syndrome ? Report of six cases and review of the literature with emphasis on ocular features(2000)33 cited
- → A Family with X-Chromosomal Recessive Congenital Cataract, Microphthalmia, a Peculiar Form of the Ear and Dental Anomalies(1979)30 cited
- → Albinism, or the NOACH syndrome(1987)27 cited
- → The Hermansky-Pudlak syndrome: Variable reaction to 1-desamino-8D-arginine vasopressin for correction of the bleeding time(1990)24 cited