Parents

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Nicolaas Marie Johannes Schweitzer grad student 1979 RUG
 (Verticale vergentie)

Children

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Frans Cornelissen grad student 1994 RUG
BETA: Related publications

Publications

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Yamada K, Andrews C, Chan WM, et al. (2003) Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). Nature Genetics. 35: 318-21
Oostra RJ, Tijmes NT, Cobben JM, et al. (1997) On the many faces of Leber hereditary optic neuropathy. Clinical Genetics. 51: 388-93
Landesz M, Worst JG, Van Rij G, et al. (1997) Opaque iris claw lens in a phakic eye to correct acquired diplopia. Journal of Cataract and Refractive Surgery. 23: 137-8
Hordijk R, Van de Logt F, Houtman WA, et al. (1996) Chorioretinal dysplasia-microcephaly-mental retardation syndrome: another family with autosomal dominant inheritance. Genetic Counseling (Geneva, Switzerland). 7: 113-22
Doorenbos-Bot ACC, Geerlings W, Houtman WA. (1996) Anterior ischemic optic neuropathy in patients undergoing hemodialysis Neuro-Ophthalmology. 16: 149-156
Engle EC, Marondel I, Houtman WA, et al. (1995) Congenital fibrosis of the extraocular muscles (autosomal dominant congenital external ophthalmoplegia): genetic homogeneity, linkage refinement, and physical mapping on chromosome 12. American Journal of Human Genetics. 57: 1086-94
de Keizer RJ, Oosterhuis JA, Houtman WA, et al. (1993) Tapioca melanoma of the iris. Annals of Ophthalmology. 25: 195-8
Kerkhof TB, Houtman WA. (1992) Late consecutive exodeviations. Documenta Ophthalmologica. Advances in Ophthalmology. 82: 65-71
Houtman WA, Roze JH, De Vries B, et al. (1991) Alternating hyperphoria. Dissociated vertical deviation (DVD) 'occlusion hyperphoria'. Documenta Ophthalmologica. Advances in Ophthalmology. 78: 135-40
Kooijman AC, Houtman WA, Assink JH, et al. (1991) Spectral sensitivity function of the a-wave of the human electroretinogram in the dark-adapted eye Clinical Vision Sciences. 6: 379-383
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