Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of LRFN5 Expression
de Bruijn, D.R.H., van Dijk, A.H.A., Pfundt, R., Hoischen, A., Merkx, G.F.M., Gradek, G.A., Lybæk, H., Stray-Pedersen, A., Brunner, H.G., Houge, G.
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Published in Molecular syndromology (01.02.2010)
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Assignment of the canalicular multispecific organic anion transporter gene (CMOAT) to human chromosome 10q24 and mouse chromosome 19d2 by fluorescent in situ hybridization
VAN KUIJCK, M. A, KOOL, M, MERKX, G. F. M, VAN KESSEL, A. G, BINDELS, R. J. M, DEEN, P. M. T, VAN OS, C. H
Published in Cytogenetic and genome research (01.01.1997)
Published in Cytogenetic and genome research (01.01.1997)
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Evidence for specificity of the DA/DAPI technique
Merkx, G F, Hopman, A H, Akkermans-Scholten, A C, Smeets, D F
Published in Cytogenetics and cell genetics (01.01.1990)
Published in Cytogenetics and cell genetics (01.01.1990)
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“Reverse” differential staining of sister chromatids
Scheres, J.M.J.C., Hustinx, Th.W.J., Rutten, F.J., Merkx, G.F.M.
Published in Experimental cell research (15.10.1977)
Published in Experimental cell research (15.10.1977)
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