Items where Author is "Baumann, B."

Article

Kohl, Susanne and Varsanyi, B. and Antunes, G. A and Baumann, B. and Hoyng, C. B. and Jagle, H. and Rosenberg, T. and Kellner, U. and Lorenz, Birgit and Salati, R. and Jurklies, B. and Farkas, A. and Andreasson, S. and Weleber, R. G. and Jacobson, S. G. and Rudolph, G. and Castellan, C. and Dollfus, H. and Legius, E. and Anastasi, M. and Bitoun, P. and Lev, D. and Sieving, P. A. and Munier, F. L. and Zrenner, E. and Sharpe, L. T. and Cremers, F. P..M. and Wissinger, Bernd (2005) CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia. EUROPEAN JOURNAL OF HUMAN GENETICS, 13 (3). pp. 302-308. ISSN 1018-4813