Moser, M. Fässler, Reinhard / Molecular Medicine, Max Planck Institute of Biochemistry, Max Planck Society;
Zerres, K., Senderek, J., Rudnik-Schoneborn, S., Eggermann, T., Kunze, J., Mononen, T., et al. (2004). New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene. Clinical Genetics, 66, 53-57.