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Works by Janvier, Ndinkabandi

Results: 4

1

Genetic Diagnosis of Duchenne and Becker Muscular Dystrophy using Multiplex Ligation-Dependent Probe Amplification in Rwandan Patients.

Published in:

Journal of Tropical Pediatrics, 2014, v. 60, n. 2, p. 112, doi. 10.1093/tropej/fmt090

By:

Uwineza, Annette;
Hitayezu, Janvier;
Murorunkwere, Seraphine;
Ndinkabandi, Janvier;
Kalala Malu, Celestin Kaputu;
Caberg, Jean Hubert;
Dideberg, Vinciane;
Bours, Vincent;
Mutesa, Leon

Publication type:

Article

2

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

Published in:

2016

By:

Uwineza, Annette;
Hitayezu, Janvier;
Jamar, Mauricette;
Caberg, Jean-Hubert;
Murorunkwere, Seraphine;
Janvier, Ndinkabandi;
Bours, Vincent;
Mutesa, Leon

Publication type:

journal article

3

A Rare Homozygous AP4S1 Variant in Rwandan Siblings with Autosomal Recessive Hereditary Spastic Paraplegia Type 52 (SPG52).

Published in:

Genes, 2025, v. 16, n. 5, p. 542, doi. 10.3390/genes16050542

By:

Niyoyita, Sylvine;
Uwibambe, Esther;
Ndinkabandi, Janvier;
Sesonga, Placide;
Niyongere, Josse Belladone;
Tuyishimire, Benjamin;
Urugwiro, Adelaide;
Rwamatwara, Alype;
Isingizwe, Gisèle;
Mutamuliza, Janvière;
Nsanzabaganwa, Christian;
Bukuru, John;
Rutagarama, Florent;
Mukaruziga, Agnès;
Karangwa, Osée;
Ndatinya, Augustin;
Nsanzabera, Maurice;
Dukuze, Norbert;
Mutesa, Léon

Publication type:

Article

4

Pattern of congenital heart diseases in Rwandan children with genetic defects.

Published in:

Pan African Medical Journal, 2014, v. 19, p. 1, doi. 10.11604/pamj.2014.19.85.3428

By:

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

Publication type:

Article