W. A. Houtman

Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)

M. Brodsky, B. Hart, J. Demer, 2003, Nature Genetics.

Congenital fibrosis of the extraocular muscles (autosomal dominant congenital external ophthalmoplegia): genetic homogeneity, linkage refinement, and physical mapping on chromosome 12.

R. Kucherlapati, D. Ward, R. Kucherlapati, 1995, American journal of human genetics.

Poly(L-lactide) implants for repair of human orbital floor defects: clinical and magnetic resonance imaging evaluation of long-term results.

F W Cordewener, F. Rozema, R. Bos, 1996, Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons.

X-linked incomplete achromatopsia with more than one class of functional cones.

J. Pokorny, V. Smith, M. Cozijnsen, 1983, Investigative ophthalmology & visual science.

Chorioretinal dysplasia-microcephaly-mental retardation syndrome: another family with autosomal dominant inheritance.

R. Hordijk, A. V. van Essen, W. A. Houtman, 1996, Genetic counseling.

On the many faces of Leber hereditary optic neuropathy

J. Cobben, E. Bleeker-Wagemakers, R. Oostra, 1997, Clinical genetics.