Authors: Pesch, K Tomiuk, J Broghammer, M Zrenner, E Apfelstedt-Sylla, E Jacobi, FK Wissinger, B Pusch, CM

Citation: K. Pesch et al., Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders, INT J MOL M, 8(1), 2001, pp. 53-58

Authors: Pusch, CM Maurer, J Ramser, J Tomiuk, J Achatz, H Pesch, K Lichtner, P Apfelstedt-Sylla, E Jacobi, FK Berger, W Meindl, A Wissinger, B

Citation: Cm. Pusch et al., Complete form of X-linked congenital stationary night blindness: Refined mapping and evidence of genetic homogeneity, INT J MOL M, 7(2), 2001, pp. 155-161

Authors: Pusch, CM Zeitz, C Brandau, O Pesch, K Achatz, H Feil, S Scharfe, C Maurer, J Jacobi, FK Pinckers, A Andreasson, S Hardcastle, A Wissinger, B Berger, W Meindl, A

Citation: Cm. Pusch et al., The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein, NAT GENET, 26(3), 2000, pp. 324-327

Authors: Jacobi, FK Broghammer, M Pesch, K Zrenner, E Berger, W Meindl, A Pusch, CM

Citation: Fk. Jacobi et al., Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1, HUM GENET, 107(1), 2000, pp. 89-91