p63 Gene Mutations in EEC Syndrome, Limb-Mammary Syndrome, and Isolated Split Hand–Split Foot Malformation Suggest a Genotype-Phenotype Correlation von van Bokhoven, Hans, Hamel, Ben C.J., Bamshad, Mike, Sangiorgi, Eugenio, Gurrieri, Fiorella, Duijf, Pascal H.G., Vanmolkot, Kaate R.J., van Beusekom, Ellen, van Beersum, Sylvia E.C., Celli, Jacopo, Merkx, Gerard F.M., Tenconi, Romano, Fryns, Jean Pierre, Verloes, Alain, Newbury-Ecob, Ruth A., Raas-Rotschild, Annick, Majewski, Frank, Beemer, Frits A., Janecke, Andreas, Chitayat, David, Crisponi, Giangiorgio, Kayserili, Hülya, Yates, John R.W., Neri, Giovanni, Brunner, Han G.

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UroVysion Compared with Cytology and Quantitative Cytology in the Surveillance of Non–Muscle-Invasive Bladder Cancer von Moonen, Paula M.J, Merkx, Gerard F.M, Peelen, Pim, Karthaus, Herbert F.M, Smeets, Dominique F.C.M, Witjes, J. Alfred

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Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA) von Koolen, D A, Nillesen, W M, Versteeg, M H A, Merkx, G F M, Knoers, N V A M, Kets, M, Vermeer, S, van Ravenswaaij, C M A, de Kovel, C G, Brunner, H G, Smeets, D, de Vries, B B A, Sistermans, E A

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A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification von Zeeuwen, Patrick L.J.M., van Vlijmen-Willems, Ivonne M.J.J., Hendriks, Wiljan, Merkx, Gerard F.M., Schalkwijk, Joost

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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 L... von 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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A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene von Kok, Yvette J.M.de, Merkx, Gerard F.M., van der Maarel, Silvère M., Huber, Irene, Malcolm, Susan, Ropers, Hans-Hilger, Cremers, Frans P.M.

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Deficiency of Either P-Glycoprotein or Breast Cancer Resistance Protein Protect against Acute Kidney Injury von Huls, Miriam, Schoeber, Joost P. H., Verfaillie, Catherine M., Luttun, Aernout, Ulloa-Montoya, Fernando, Menke, Aswin L., Van Bolderen, Lars R., Woestenenk, Rob M., Merkx, Gerard F. M., Wetzels, Jack F. M., Russel, Frans G. M., Masereeuw, Rosalinde

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Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families von LEMMINK, H. H, VAN DEN HEUVEL, L. P. W. J, VAN DIJK, H. A, MERKX, G. F. M, SMILDE, T. J, TASCHNER, P. E. M, MONNENS, L. A. H, HEBERT, S. C, KNOERS, N. V. A. M

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Deficiency of either P-glycoprotein or breast cancer resistance protein protect against acute kidney injury (Retraction of Vol 10, Pg 1195, 2010) von Huls, M., Schoeber, J. P., Verfaillie, C. M., Luttun, A., Ulloa-Montoya, F., Menke, A. L., Van Bolderen, L. R., Woestenenk, R. M., Merkx, G. F., Wetzels, J. F., Russel, F. G.

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Expertise in research integration and implementation for tackling complex problems: when is it needed, where can it be found and how can it be strengthened? von Bammer, Gabriele, O’Rourke, Michael, O’Connell, Deborah, Neuhauser, Linda, Midgley, Gerald, Klein, Julie Thompson, Grigg, Nicola J., Gadlin, Howard, Elsum, Ian R., Bursztyn, Marcel, Fulton, Elizabeth A., Pohl, Christian, Smithson, Michael, Vilsmaier, Ulli, Bergmann, Matthias, Jaeger, Jill, Merkx, Femke, Vienni Baptista, Bianca, Burgman, Mark A., Walker, Daniel H., Young, John, Bradbury, Hilary, Crawford, Lynn, Haryanto, Budi, Pachanee, Cha-aim, Polk, Merritt, Richardson, George P.

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Retracted: Deficiency of Either P-Glycoprotein or Breast Cancer Resistance Protein Protect against Acute Kidney Injury von Huls, Miriam, Schoeber, Joost P. H., Verfaillie, Catherine M., Luttun, Aernout, Ulloa-Montoya, Fernando, Menke, Aswin L., Van Bolderen, Lars R., Woestenenk, Rob M., Merkx, Gerard F. M., Wetzels, Jack F. M., Russel, Frans G. M., Masereeuw, Rosalinde

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Linear binary code for write-once memories (Corresp.) von Cohen, G., Godlewski, P., Merkx, F.

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ICF syndrome : a new case and review of the literature von SMEETS, D. F. C. M, MOOG, U, WEEMAES, C. M. R, VAES-PEETERS, G, MERKX, G. F. M, NIEHOF, J. P, HAMERS, G

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Assignment of the human adipocyte fatty acid-binding protein gene (FABP4) to chromosome 8q21 using somatic cell hybrid and fluorescence in situ hybridization techniques von PRINSEN, C. F. M, DE BRUIJN, D. R. H, MERKX, G. F. M, VEERKAMP, J. H

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cDNA Cloning and Chromosomal Localization of the Genes Encoding the α- and β-Subunits of Human Rab Geranylgeranyl Transferase: The 3′ End of the α-Subunit Gene Overlaps with the Tr... von Bokhoven, Hans Van, Rawson, Robert B., Merkx, Gerard F.M., Cremers, Frans P.M., Seabra, Miguel C.

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Gene Structure and Chromosomal Mapping of Human Epithelial Calcium Channel von Müller, Dominik, Hoenderop, Joost G.J., Merkx, Gerard F.M., van Os, Carel H., Bindels, René J.M.

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Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes von Smeets, D F, Merkx, G F, Hopman, A H

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Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent von Van Der Burgt, C J, Merkx, G F, Janssen, A H, Mulder, J C, Suijkerbuijk, R F, Smeets, D F

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Urovysion compared with cytology and quantitative cytology in the surveillance of non-muscle-invasive bladder cancer. Commentary von MOONEN, Paula M. J, MERKX, Gerard F. M, PEELEN, Pim, KARTHAUS, Herbert F. M, SMEETS, Dominique F. C. M, WITJES, J. Alfred, VAN RHIJN, Bas W. G

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Expertise in research integration and implementation for tackling complex problems: when is it needed, where can it be found and how can it be strengthened? von Bammer, G, O'Rourke, M, O'Connell, D, Neuhauser, L, Midgley, G, Klein, JT, Grigg, NJ, Gadlin, H, Elsum, IR, Bursztyn, M, Fulton, EA, Pohl, C, Smithson, M, Vilsmaier, U, Bergmann, M, Jaeger, J, Merkx, F, Baptista, BV, Burgman, MA, Walker, DH, Young, J, Bradbury, H, Crawford, L, Haryanto, B, Pachanee, C-A, Polk, M, Richardson, GP

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