S. Spranger
Center for Human Genetics and Genetic Counseling
University of Bremen
Germany
Name/email consistency: high
- Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3. Spranger, S., Schiller, S., Jauch, A., Wolff, K., Rauterberg-Ruland, I., Hager, D., Tariverdian, G., Tröger, J., Rappold, G. Am. J. Med. Genet. (1999)