Browse by ["viewname_eprint_publisher" not defined]

R

Ragge, N.K and Brown, A. G. and Poloschek, Charlotte M. and Lorenz, Birgit and Henderson, R.A. and Clarke, M. P. and Russell-Eggitt, I. and Fielder, A. and Gerrelli, D. and Martinez-Barbera, J. P. and Ruddle, P. and Hurst, J. and Collin, J. R. O. and Salt, A. and Cooper, S. T. and Thompson, P. J. and Sisodiya, S. M. and Williamson, K. A. and FitzPatrick, D. R. and van Heyningen, V. and Hanson, I.M . (2005) Heterozygous mutations of OTX2 cause severe ocular malformations. AMERICAN JOURNAL OF HUMAN GENETICS, 76 (6). pp. 1008-1022. ISSN 0002-9297, 1537-6605

W

Wissinger, Bernd and Gamer, Daphne and Jaegle, Herbert and Giorda, Roberto and Marx, Tim and Mayer, Simone and Tippmann, Sabine and Broghammer, Martina and Jurklies, Bernhard and Rosenberg, Thomas and Jacobson, Samuel G. and Sener, E. Cumhur and Tatlipinar, Sinan and Hoyng, Carel B. and Castellan, Claudio and Bitoun, Pierre and Andreasson, Sten and Rudolph, Günter and Kellner, Ulrich and Lorenz, Birgit and Wolff, Gerhard and Verellen-Dumoulin, Christine and Schwartz, Marianne and Cremers, Frans P. M. and Apfelstedt-Sylla, Eckart and Zrenner, Eberhart and Salati, Roberto and Sharpe, Lindsay T. and Kohl, Susanne (2001) CNGA3 mutations in hereditary cone photoreceptor disorders. AMERICAN JOURNAL OF HUMAN GENETICS, 69 (4). pp. 722-737. ISSN 0002-9297, 1537-6605