Showing results (1-10 of 232) with videos related to
Sort By:
Pageof 24
Archives of Dermatology|December 1, 1984
Neurofibromatosis and hypertelorismW Westerhof, J W Delleman, E Wolters, et al.Neuropediatrics|November 1, 1986
Hypertelorism in neurofibromatosisE C Wolters, W Westerhof, J W Delleman, 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.Archives of Dermatology|June 1, 1978
Hereditary congenital hypopigmented and hyperpigmented maculesW Westerhof, F A Beemer, R H Cormane, et al.American Journal of Human Genetics|September 1, 1977
Heterogeneity in Waardenburg syndromeM J Hageman, J W DellemanJournal of Pediatric Ophthalmology and Strabismus|November 1, 1978
Ophthalmological findings in 34 patients with Waardenburg syndromeJ W Delleman, M J HagemanOphthalmic Paediatrics and Genetics|June 1, 1992
Autosomal dominant congenital miosis with megalocorneaF M Meire, J W DellemanThe British Journal of Ophthalmology|October 1, 1994
Biometry in X linked megalocornea: pathognomonic findingsF M Meire, J W DellemanThe British Journal of Ophthalmology|June 1, 1988
Familial grouped pigmentation of the retinal pigment epitheliumP T de Jong, J W DellemanJournal 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 DellemanPageof 24