Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndrome

Por van Haelst, M M, Eussen, H, Visscher, F, de Ruijter, J L M, Drop, S, Lindhout, D, Wouters, C, Govaerts, L
Publicado em 2002

Savings and extinction of conditioned eyeblink responses in fragile X syndrome

Por Smit, A E, van der Geest, J N, Vellema, M, Koekkoek, S K E, Willemsen, R, Govaerts, L C P, Oostra, B A, De Zeeuw, C I, VanderWerf, F
Publicado em 2008

The fragile X syndrome: no evidence for any recent mutations.

Por Smits, A P, Dreesen, J C, Post, J G, Smeets, D F, de Die-Smulders, C, Spaans-van der Bijl, T, Govaerts, L C, Warren, S T, Oostra, B A, van Oost, B A
Publicado em 1993

The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents’ Experiences

Por van der Steen, S. L., Riedijk, S. R., Verhagen-Visser, J., Govaerts, L. C. P., Srebniak, M. I., Van Opstal, D., Joosten, M., Knapen, M. F. C. M., Tibben, A., Diderich, K. E. M., Galjaard, R. J. H.
Publicado no J Genet Couns (2016)

Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.

Por Warburton, P E, Dolled, M, Mahmood, R, Alonso, A, Li, S, Naritomi, K, Tohma, T, Nagai, T, Hasegawa, T, Ohashi, H, Govaerts, L C, Eussen, B H, Van Hemel , J O, Lozzio, C, Schwartz, S, Dowhanick-Morrissette, J J, Spinner, N B, Rivera, H, Crolla, J A, Yu, C, Warburton, D
Publicado em 2000

Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?

Por van der Steen, S. L., Bunnik, E. M., Polak, M. G., Diderich, K. E. M., Verhagen-Visser, J., Govaerts, L. C. P., Joosten, M., Knapen, M. F. C. M., Go, A. T. J. I., Van Opstal, D., Srebniak, M. I., Galjaard, R. J. H., Tibben, A., Riedijk, S. R.
Publicado no J Genet Couns (2017)