Medical genetics and genomic medicine in Rwanda

Por Uwineza, Annette, Mutesa, Leon
Publicado no Mol Genet Genomic Med (2015)

Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies

Por Uwineza, Annette, Hitayezu, Janvier, Jamar, Mauricette, Caberg, Jean-Hubert, Murorunkwere, Seraphine, Janvier, Ndinkabandi, Bours, Vincent, Mutesa, Leon
Publicado no J Trop Pediatr (2016)

Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies

Por Uwineza, Annette, Caberg, Jean-Hubert, Hitayezu, Janvier, Hellin, Anne Cecile, Jamar, Mauricette, Dideberg, Vinciane, Rusingiza, Emmanuel K, Bours, Vincent, Mutesa, Leon
Publicado em 2014

Adherence to Highly Active Antiretroviral Treatment in HIV-Infected Rwandan Women

Por Musiime, Stephenson, Muhairwe, Fred, Rutagengwa, Alfred, Mutimura, Eugene, Anastos, Kathryn, Hoover, Donald R., Qiuhu, Shi, Munyazesa, Elizaphane, Emile, Ivan, Uwineza, Annette, Cowan, Ethan
Publicado em 2011

Pattern of congenital heart diseases in Rwandan children with genetic defects

Por Teteli, Raissa, Uwineza, Annette, Butera, Yvan, Hitayezu, Janvier, Murorunkwere, Seraphine, Umurerwa, Lamberte, Ndinkabandi, Janvier, Hellin, Anne-Cécile, Jamar, Mauricette, Caberg, Jean-Hubert, Muganga, Narcisse, Mucumbitsi, Joseph, Rusingiza, Emmanuel Kamanzi, Mutesa, Leon
Publicado no Pan Afr Med J (2014)

Limb body wall complex, amniotic band sequence, or new syndrome caused by mutation in IQ Motif containing K (IQCK)?

Por Kruszka, Paul, Uwineza, Annette, Mutesa, Leon, Martinez, Ariel F, Abe, Yu, Zackai, Elaine H, Ganetzky, Rebecca, Chung, Brian, Stevenson, Roger E, Adelstein, Robert S, Ma, Xuefei, Mullikin, James C, Hong, Sung-Kook, Muenke, Maximilian
Publicado no Mol Genet Genomic Med (2015)

22q11.2 Deletion Syndrome in Diverse Populations

Por Kruszka, Paul, Addissie, Yonit A., McGinn, Daniel E., Porras, Antonio R., Biggs, Elijah, Share, Matthew, Crowley, T. Blaine, Chung, Brian H.Y., Mok, Gary T.K., Mak, Christopher CY, Muthukumarasamy, Premala, Thong, Meow-Keong, Sirisena, Nirmala D., Dissanayake, Vajira H.W., Paththinige, C. Sampath, Prabodha, L.B. Lahiru, Mishra, Rupesh, Shotelersuk, Vorasuk, Ekure, Ekanem Nsikak, Sokunbi, Ogochukwu Jidechukwu, Kalu, Nnenna, Ferreira, Carlos R., Duncan, Jordann-Mishael, Patil, Siddaramappa Jagdish, Jones, Kelly L., Kaplan, Julie D., Abdul-Rahman, Omar A., Uwineza, Annette, Mutesa, Leon, Moresco, Angélica, Obregon, María Gabriela, Richieri-Costa, Antonio, Gil-da-Silva-Lopes, Vera L, Adeyemo, Adebowale A., Summar, Marshall, Zackai, Elaine H., McDonald-McGinn, Donna M., Linguraru, Marius George, Muenke, Maximilian
Publicado no Am J Med Genet A (2017)