Mental Retardation in Amaurosis Congenita of Leber von Schuil, J., Meire, F. M., Delleman, J. W.

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Biometry in X linked megalocornea: pathognomonic findings von Meire, F M, Delleman, J W

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Long term ocular and neurological involvement in severe congenital toxoplasmosis von Meenken, C, Assies, J, van Nieuwenhuizen, O, Holwerda-van der Maat, W G, van Schooneveld, M J, Delleman, W J, Kinds, G, Rothova, A

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X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysis von Meire, F M, Bergen, A A, De Rouck, A, Leys, M, Delleman, J W

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The intraocular straylight function in some hereditary corneal dystrophies von VAN DEN BERG, T. J. T. P, HWAN, B. S, DELLEMAN, J. W

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Additional Evidence for a Gene Locus for Progressive Cone Dystrophy with Late Rod Involvement in Xp21.1-p11.3 von Bergen, Arthur A.B., Meire, Francoise, ten Brink, Jacoline, Schuurman, Ellen J.M., van Ommen, Gert-Jan B., Delleman, J.Willem

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Familial grouped pigmentation of the retinal pigment epithelium von de Jong, P T, Delleman, J W

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Autosomal Dominant Congenital Miosis with Megalocornea von Meire, F. M., Delleman, J. W.

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Heterogeneity in Waardenburg syndrome von Hageman, M J, Delleman, J W

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Crystalline cataract and uncombable hair. Ultrastructural and biochemical findings von DE JONG, P. T. V. M, BLEEKER-WAGEMAKERS, E. M, VRENSEN, G. F. J. M, BROEKHUYSE, R. M, PEEREBOOM-WYNIA, J. D. R, DELLEMAN, J. W

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Hypertelorism in Neurofibromatosis von Wolters, E. Ch, Westerhof, W., Delleman, J. W., Dijkstra, P.

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X-linked megalocornea Ocular findings and linkage analysis von Meire, F. M., Bleeker-Wagemakers, E. M., Oehler, M., Gal, A., Delleman, J. W.

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A discussion of 61 cases of optic nerve coloboma von VAN DALEN, J. T. W, DELLEMAN, J. W, YOGIANTORO, M

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Pigment epithelial pattern dystrophy: a peripheral type von Delleman, J W, de Jong, P T

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Albinism: phenotype or genotype? von VAN DORP, D. B, VAN HAERINGEN, N. J, DELLEMAN, J. W, APKARIAN, P, WESTERHOF, W

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Ito's hypomelanosis (incontinentia pigmenti achromians): A review of four cases von Fleury, P., Dingemans, K., de Groot, W.P., Oranje, A.P., Voûte, P.A., Woerdeman, M.J., Delleman, J.W., Oorthuys, J.W.E., Verboom, A.J.

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Peters'-Plus: A new syndrome von Van Schooneveld, M. J., Delleman, J. W., Beemer, F. A., Bleeker-Wagemakerp, E. M.

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X-linked incomplete achromatopsia with more than one class of functional cones von Smith, V C, Pokorny, J, Delleman, J W, Cozijnsen, M, Houtman, W A, Went, L N

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Usher's syndrome, temporal bone pathology von Cremers, Cor W.R.J., Delleman, Willem J.W.

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Ocular manifestations of congenital Marfan syndrome with contractures (CMC syndrome) von Meire, Françhise M., Delleman, Willem J., Bleeker-Wagemakers, Elisabeth M.

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