Freeman–Sheldon Syndrome: First Molecularly Confirmed Case from Sub-Saharan Africa

por Ali, A. M., Mbwasi, R. M., Kinabo, G., Kamsteeg, E.-J., Hamel, B. C., Dekker, M. C. J.
Publicado 2017

Jeune syndrome: description of 13 cases and a proposal for follow-up protocol

por de Vries, J., Yntema, J. L., van Die, C. E., Crama, N., Cornelissen, E. A. M., Hamel, B. C. J.
Publicado 2009

Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter–22q11.2

por Hulsebos, T J M, Oskam, N T, Bijleveld, E H, Westerveld, A, Hermsen, M A, Ouweland, A M W van den, Hamel, B C
Publicado 1999

A Tanzanian Boy with Molecularly Confirmed X-Linked Adrenoleukodystrophy

por Dekker, M. C. J., Sadiq, A. M., Mc Larty, R., Mbwasi, R. M., Willemsen, M. A. A. P., Waterham, H. R., Hamel, B. C.
Publicado 2019