Lived Experiences of Fragile X Syndrome Caregivers: A Scoping Review of Qualitative Studies

Yazar: Kamga, Karen Kengne, De Vries, Jantina, Nguefack, Seraphin, Munung, Syntia Nchangwi, Wonkam, Ambroise
Yayımlandı Front Neurol (2020)

Stakeholder Perspectives on Public Health Genomics Applications for Sickle Cell Disease: A Methodology for a Human Heredity and Health in Africa (H3Africa) Qualitative Research Stu...

Yazar: Treadwell, Marsha J., Makani, Julie, Ohene-Frempong, Kwaku, Ofori-Acquah, Solomon, McCurdy, Sheryl, de Vries, Jantina, Bukini, Daima, Dennis-Antwi, Jemima, Kamga, Karen Kengne, Mbekenga, Columba, Wonkam, Edmond Tingang, Tangwa, Godfrey, Royal, Charmaine D., Wonkam, Ambroise
Yayımlandı OMICS (2017)

Proceedings of a Sickle Cell Disease Ontology workshop — Towards the first comprehensive ontology for Sickle Cell Disease

Yazar: Mulder, Nicola, Nembaware, Victoria, Adekile, Adekunle, Anie, Kofi A., Inusa, Baba, Brown, Biobele, Campbell, Andrew, Chinenere, Furahini, Chunda-Liyoka, Catherine, Derebail, Vimal K., Geard, Amy, Ghedira, Kais, Hamilton, Carol M., Hanchard, Neil A., Haendel, Melissa, Huggins, Wayne, Ibrahim, Muntaser, Jupp, Simon, Kamga, Karen Kengne, Knight-Madden, Jennifer, Lopez-Sall, Philomène, Mbiyavanga, Mamana, Munube, Deogratias, Nirenberg, Damian, Nnodu, Obiageli, Ofori-Acquah, Solomon Fiifi, Ohene-Frempong, Kwaku, Opap, Kenneth Babu, Panji, Sumir, Park, Miriam, Pule, Gift, Royal, Charmaine, Sangeda, Raphael, Tayo, Bamidele, Treadwell, Marsha, Tshilolo, Léon, Wonkam, Ambroise
Yayımlandı Appl Transl Genom (2016)