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

per Sitorus, R, Preising, M, Lorenz, B
Publicat 2003

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

per Sitorus, R, Ardjo, S, Lorenz, B, Preising, M
Publicat 2003

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

per Heegaard, S, Rosenberg, T, Preising, M, Prause, J U, Bek, T
Publicat 2003

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

per Preising, M., de Laak, J.-P. O., Lorenz, B.
Publicat 2001

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

per Schindler, S, Friedrich, M, Wagener, H, Lorenz, B, Preising, M
Publicat 2002

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

per Preising, M. N., Friedburg, C., Bowl, W., Lorenz, B.
Publicat a Biomed Res Int (2018)