B. V. D. Helm

A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family.

H. Kremer, B. Hamel, H. Kremer, 1999, American journal of human genetics.

Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch family.

J. Leunissen, H. Kremer, B. Hamel, 1996, Human molecular genetics.

A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

H. Brunner, F. Cremers, S. Yzer, 2003, Journal of medical genetics.

Localization of the gene for dominant cystoid macular dystrophy on chromosome 7p.

A. Deutman, H. Kremer, H. Ropers, 1994, Human molecular genetics.