Results: 1-3 |
Results: 3

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: Rudolph, G Meindl, A Bechmann, M Schworm, HD Achatz, H Boergen, KP Kampik, A Berninger, T Meitinger, T
Citation: G. Rudolph et al., X-linked ocular albinism (Nettleship-falls): a novel 29-bp deletion in exon 1. Carrier detection by ophthalmic examination and DNA analysis, GR ARCH CL, 239(3), 2001, pp. 167-172

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
Risultati: 1-3 |