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D B van Dorp

Showing results (1-10 of 21) with videos related to

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American Journal of Ophthalmology|November 1, 1984
Albinotic characteristics in congenital nystagmusD B van Dorp
Clinical Genetics|April 1, 1987
Albinism, or the NOACH syndrome (the book of Enoch c.v. 1-20)D B van Dorp
Ophthalmic Paediatrics and Genetics|June 1, 1990
Tuberous sclerosis. Diagnostic problems in a familyD B van Dorp, M L Kwee
American Journal of Hematology|March 1, 1989
Hermansky-Pudlak syndrome: correction of bleeding time by 1-desamino-8D-arginine vasopressinP W Wijermans, D B van Dorp
Journal of Pediatric Ophthalmology and Strabismus|May 1, 1979
A family with X-chromosomal recessive congenital cataract, microphthalmia, a peculiar form of the ear and dental anomaliesD B van Dorp, J W Delleman
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1991
X-linked congenital stationary night blindness: review and report of a family with hyperopiaA F Wright, D B van Dorp
Ophthalmic Paediatrics and Genetics|February 1, 1985
Fluorescein angiography in potential carriers for choroideremia. An additional aid for final diagnosis, when funduscopy shows equivocal symptomsD B van Dorp, A T van Balen
Clinical Genetics|November 1, 1984
Oculocutaneous albinism and anterior chambre cleavage malformations. Not a coincidenceD B van Dorp, J W Delleman, D H Loewer-Sieger
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.
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.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
American Journal of Ophthalmology|November 1, 1984
Albinotic characteristics in congenital nystagmusD B van Dorp
Clinical Genetics|April 1, 1987
Albinism, or the NOACH syndrome (the book of Enoch c.v. 1-20)D B van Dorp
Ophthalmic Paediatrics and Genetics|June 1, 1990
Tuberous sclerosis. Diagnostic problems in a familyD B van Dorp, M L Kwee
American Journal of Hematology|March 1, 1989
Hermansky-Pudlak syndrome: correction of bleeding time by 1-desamino-8D-arginine vasopressinP W Wijermans, D B van Dorp
Journal of Pediatric Ophthalmology and Strabismus|May 1, 1979
A family with X-chromosomal recessive congenital cataract, microphthalmia, a peculiar form of the ear and dental anomaliesD B van Dorp, J W Delleman
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1991
X-linked congenital stationary night blindness: review and report of a family with hyperopiaA F Wright, D B van Dorp
Ophthalmic Paediatrics and Genetics|February 1, 1985
Fluorescein angiography in potential carriers for choroideremia. An additional aid for final diagnosis, when funduscopy shows equivocal symptomsD B van Dorp, A T van Balen
Clinical Genetics|November 1, 1984
Oculocutaneous albinism and anterior chambre cleavage malformations. Not a coincidenceD B van Dorp, J W Delleman, D H Loewer-Sieger
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.
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.
Pageof 3