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Ophthalmic Paediatrics and Genetics|September 1, 1990
The Hermansky-Pudlak syndrome. Variable reaction to 1-desamino-8D-arginine vasopressin for correction of the bleeding timeD B Van Dorp, P W Wijermans, F Meire, et al.
Knee Surgery & Related Research|September 18, 2014
Popliteal pseudoaneurysm after arthroscopic posterior cruciate ligament reconstructionKarin B van Dorp, Stefan J M Breugem, Marcel J M Driessen
Nucleic Acids Research|May 1, 1978
A cell-free system for the replication fo bacteriophage M-13 duplex DNAP K Schneck, B van Dorp, W L Staudenbauer, et al.
World Journal of Orthopedics|April 27, 2016
Promising short-term clinical results of the cementless Oxford phase III medial unicondylar knee prosthesisKarin B van Dorp, Stefan Jm Breugem, Daniël J Bruijn, et al.
Human Genetics|January 1, 1992
A family with RP3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalitiesD B van Dorp, A F Wright, A D Carothers, et al.
The Journal of Foot and Ankle Surgery : Official Publication of the American College of Foot and Ankle Surgeons|November 2, 2010
Chopart joint injury: a study of outcome and morbidityKarin B van Dorp, Mark R de Vries, Maarten van der Elst, et al.
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.
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