![]() ![]() | Uwineza, A. (2015). Etude des étiologies génétiques de la déficience intellectuelle chez des patients Rwandais [Doctoral thesis, Université de Liège]. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/314890 |
![]() ![]() | Uwineza, A., BULK, S., CABERG, J.-H., & PIERQUIN, G. (06 March 2015). A new case of microdeletion 14q32.3 [Poster presentation]. 15th Belgium Society of Human Genetics Meeting, Charleroi, Belgium. |
![]() ![]() | Teteli, R., Uwineza, A., Butera, Y., Hitayezu, J., Murorunkwere, S., Umurerwa, L., Ndinkabandi, J., Hellin, A.-C., JAMAR, M., CABERG, J.-H., Muganga, N., Mucumbitsi, J., Rusingiza, E. K., & Mutesa, L. (2014). Pattern of congenital heart diseases in Rwandan children with genetic defects. Pan African Medical Journal, 19, 85. doi:10.11604/pamj.2014.19.85.3428 ![]() |
![]() ![]() | Uwineza, A., Hitayezu, J., Murorunkwere, S., Ndinkabandi, J., Kalala Malu, C. K., CABERG, J.-H., DIDEBERG, V., BOURS, V., & Mutesa, L. (2013). Genetic diagnosis of Duchenne and Becker muscular dystrophy using multiplex ligation-dependent probe amplification in Rwandan patients. Journal of Tropical Pediatrics. doi:10.1093/tropej/fmt090 ![]() |
![]() ![]() | Uwineza, A., PIERQUIN, G., GAILLEZ, S., JAMAR, M., CABERG, J.-H., & BOURS, V. (2013). Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13. Genetic Counseling, 24 (2), 193-200. ![]() |