DMD‐related muscular dystrophy in Cameroon: Clinical and genetic profiles

por Wonkam‐Tingang, Edmond, Nguefack, Séraphin, Esterhuizen, Alina I., Chelo, David, Wonkam, Ambroise
Publicado 2020

Noonan Syndrome in South Africa: Clinical and Molecular Profiles

por Tekendo-Ngongang, Cedrik, Agenbag, Gloudi, Bope, Christian Domilongo, Esterhuizen, Alina Izabela, Wonkam, Ambroise
Publicado 2019

Clinical Application of Epilepsy Genetics in Africa: Is Now the Time?

por Esterhuizen, Alina I., Carvill, Gemma L., Ramesar, Rajkumar S., Kariuki, Symon M., Newton, Charles R., Poduri, Annapurna, Wilmshurst, Jo M.
Publicado 2018

Cascade Testing for Fragile X Syndrome in a Rural Setting in Cameroon (Sub-Saharan Africa)

por Kengne Kamga, Karen, Nguefack, Séraphin, Minka, Khuthala, Wonkam Tingang, Edmond, Esterhuizen, Alina, Nchangwi Munung, Syntia, De Vries, Jantina, Wonkam, Ambroise
Publicado 2020