Items where Author is "Chrast, R."
Number of items: 2. 2016Nikopoulos, K. and Butt, G. U. and Farinelli, P. and Mudassar, M. and Domènech-Estévez, E. and Samara, C. and Kausar, M. and Masroor, I. and Chrast, R. and Rivolta, C. and Siddiqi, S.. (2016) A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani family. Clinical Genetics, 89 (4). pp. 510-511. 2012Azzedine, H. and Senderek, J. and Rivolta, C. and Chrast, R.. (2012) Molecular genetics of charcot-marie-tooth disease: from genes to genomes. Molecular syndromology, 3 (5). pp. 204-214. |
