Willem A Houtman

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

Koki Yamada, Caroline Andrews, Wai‐Man Chan et al. · Nature Genetics · 2003 · 262 citations

Medicine, Genetics, Molecular Genetics +14

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

F. W. Cordewener, R. Bös, Fred R. Rozema et al. · Journal of Oral and Maxillofacial Surgery · 1996 · 107 citations

Medicine, Surgery, Implant Surgery +13

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

Elizabeth C. Engle, Ivonne Marondel, Willem A Houtman et al. · PubMed · 1995 · 82 citations

Medicine, Genetics, Ophthalmology +15

Hereditary Congenital External Ophthalmoplegia

Willem A Houtman, T.W. van Weerden, P. H. Robinson et al. · Ophthalmologica · 2010 · 21 citations

Medicine, Neurology, Ophthalmology +11