Bergmann, C., J. Senderek, F. Küpper, F. Schneider, C. Dornia, E. Windelen, T. Eggermann, S. Rudnik-Schöneborn, J. Kirfel, L. Furu, L. E. Onuchic, S. Rossetti, P. C. Harris, S. Somlo, L. Guay-Woodford, G. G. Germino, M. Moser, R. Büttner and K. Zerres: PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD). In: Human Mutation 23, 5, 453-463 (2004).
Bergmann, C., J. Senderek, F. Schneider, C. Dornia, F. Kupper, T. Eggermann, S. Rudnik-Schöneborn, J. Kirfel, M. Moser, R. Büttner and K. Zerres: PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD). In: Human Mutation 23, 5, 487-495 (2004).
http://edoc.mpg.de
The Max Planck Society does not take any responsibility for the content of this export.