Causes of blindness at the “Wiyata Guna” School for the Blind, Indonesia

by Sitorus, R, Preising, M, Lorenz, B
Published 2003

CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients

by Sitorus, R, Ardjo, S, Lorenz, B, Preising, M
Published 2003

An unusual retinal vascular morphology in connection with a novel AIPL1 mutation in Leber’s congenital amaurosis

by Heegaard, S, Rosenberg, T, Preising, M, Prause, J U, Bek, T
Published 2003

Deletion in the OA1 gene in a family with congenital X linked nystagmus

by Preising, M., de Laak, J.-P. O., Lorenz, B.
Published 2001

Heterozygous P250L mutation of fibroblast growth factor receptor 3 in a case of isolated craniosynostosis

by Schindler, S, Friedrich, M, Wagener, H, Lorenz, B, Preising, M
Published 2002

Unexpected Genetic Cause in Two Female Siblings with High Myopia and Reduced Visual Acuity

by Preising, M. N., Friedburg, C., Bowl, W., Lorenz, B.
Published in Biomed Res Int (2018)