Clinical heterogeneity and novel mutations in the glycerol kinase gene in three families with isolated glycerol kinase deficiency.

Por Sjarif, D R, Sinke, R J, Duran, M, Beemer, F A, Kleijer, W J, Ploos van Amstel, J K, Poll-The, B T
Publicado em 1998

Cloning, chromosomal localization, and functional expression of the alpha 1 subunit of the L-type voltage-dependent calcium channel from normal human heart.

Por Schultz, D, Mikala, G, Yatani, A, Engle, D B, Iles, D E, Segers, B, Sinke, R J, Weghuis, D O, Klöckner, U, Wakamori, M
Publicado em 1993

A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q

Por Bakker, S. C., Meulen, E. M. van der, Buitelaar, J. K., Sandkuijl, L. A., Pauls, D. L., Monsuur, A. J., Slot, R. van ‘t, Minderaa, R. B., Gunning, W. B., Pearson, P. L., Sinke, R. J.
Publicado em 2003

Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing

Por Johansson, L. F., de Boer, E. N., de Weerd, H. A., van Dijk, F., Elferink, M. G., Schuring-Blom, G. H., Suijkerbuijk, R. F., Sinke, R. J., te Meerman, G. J., Sijmons, R. H., Swertz, M. A., Sikkema-Raddatz, B.
Publicado no Sci Rep (2017)