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Ophthalmic 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 DellemanNeuropediatrics|February 24, 1999
Mental retardation in amaurosis congenita of LeberJ Schuil, F M Meire, J W DellemanOphthalmic Paediatrics and Genetics|September 1, 1991
X-linked megalocornea. Ocular findings and linkage analysisF M Meire, E M Bleeker-Wagemakers, M Oehler, et al.The British Journal of Ophthalmology|February 1, 1994
X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysisF M Meire, A A Bergen, A De Rouck, 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 HagemanBulletin De La Societe Belge D'Ophtalmologie|January 1, 1991
Hereditary ectopia lentis. A series of 10 cases of ectopia lentis et pupillaeF M MeireThe 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 6