References
- De Jong J. G. Y., Delleman J. W., Houben M., Manschot W. A., De Minjer A., Mol J., Slooff J. L. Agenesis of the corpus callosum, infantile spasms, ocular anomalies (Aicardi syndrome). Neurology 1976; 26: 1152–1158
- Delleman J. W., Winkelman J. E. Die Bedeutung der atypischen Kolobome und Defekte der Iris fur die Erkennung des hereditaren Aniridie-Syndroms. Klin. Mbl. Augenheilk. 1973; 163: 5
- Delleman J. E., De Jong J. G. Y., Bleeker G. M. Meningiomas in five members of a family over two generations, in one member simultaneously with acoustic neurinomas. Neurology 1978; 25: 567–570
- Van Dalen J. T. W., Delleman J. W., Loewer-Sieger D. H. Optic nerve hypoplasia. Neurogenetics and N euro-ophthalmology, A. Huberand, D. Klein. Elsevier/North-Holland Biomedical Press, Amsterdam 1981; 253–257
- Van Dorp D., Delleman J. W. A family with X-chromosomal recessive congenital cataract, microphthalmia, a peculiar form of the ear and dental anomalies. J. ped. Ophthal. Strabismus 1979; 16: 166–171
- Van Went J. J., Van Went G. F., Delleman J. W., Becker A. G. Spina bifida and so-called asplenia syndrome occurring separately in sibs. Teratology 1977; 15: 195–198