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Uwineza Annette

Main Referenced Co-authors
Caberg, Jean-Hubert  (4)
Bours, Vincent  (2)
Hitayezu, Janvier (2)
Jamar, Mauricette  (2)
Murorunkwere, Seraphine (2)
Main Referenced Keywords
Rwanda (3); Abnormalities, Multiple/genetics (1); Adolescent (1); Adult (1); Africa (1);
Main Referenced Disciplines
Genetics & genetic processes (5)

Publications (total 5)

The most downloaded
251 downloads
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. https://hdl.handle.net/2268/160353

The most cited

8 citations (OpenCitations)

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 https://hdl.handle.net/2268/165763

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
Peer reviewed

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.
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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