Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation

by Bronwyn Dillon, Candice Feben, David Segal, Johannes duPlessis, David Reynders, Rosalind Wainwright, Janet Poole, Amanda Krause
Published 2020-08-01

Ending a diagnostic odyssey—The first case of Takenouchi–Kosaki syndrome in an African patient

by Kaitlyn Flynn, Candice Feben, Lindiwe Lamola, Nadia Carstens, Amanda Krause, Zané Lombard, for DDD‐Africa as members of the H3Africa Consortium
Published 2021-04-01