High-resolution in situ hybridization using DNA halo preparations von Wiegant, J., Kalle, W., Mullenders, L., Brookes, S., Hoovers, J.M.N., Dauwerse, J.G., van Ommen, G.J.B., Raap, A.K.

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Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16) von GILES, R. H, DAUWERSE, J. G, VAN OMMEN, G.-J. B, HAGEMEIJER, A, VAN DER REIJDEN, B. A, BREUNING, M. H, HIGGINS, C, PETRIJ, F, WESSELS, J. W, BEVERSTOCK, G. C, DÖHNER, H, JOTTERAND-BELLOMO, M, FALKENBURG, J. H. F, SLATER, R. M

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Multiple colors by fluorescence in situ hybridization using ratio-labelled DNA probes create a molecular karyotype von Dauwerse, J.G., Wiegant, J., Raap, A.K., Breuning, M.H., van Ommen, G.J.B.

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Heterozygous truncating mutation in the human homeobox gene GSH2 has no discernable phenotypic effect von Dauwerse, J G, de Die-Smulders, C E M, Bakker, E, Breuning, M H, Peters, D J M

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Acrofacial dysostosis in a patient with the TSC2-PKD1 contiguous gene syndrome von Dauwerse, J G, Bouman, K, van Essen, A J, van der Hout, A H, Kolsters, G, Breuning, M H, Peters, D J M

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A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region von Baysal, B E, Willett-Brozick, J E, Taschner, P E, Dauwerse, J G, Devilee, P, Devlin, B

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High susceptibility of chromosome 16 to radiation-induced chromosome rearrangements in human lymphocytes under in vivo and in vitro exposure von Camparoto, M.L., Takahashi-Hyodo, S.A., Dauwerse, J.G., Natarajan, A.T., Sakamoto-Hojo, E.T.

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Extensive Cross-Homology Between the Long and the Short Arm of Chromosome 16 May Explain Leukemic Inversions and Translocations von Dauwerse, J.G., Jumelet, E.A., Wessels, J.W., Saris, J.J., Hagemeijer, A., Beverstock, G.C., Ommen, G.J.B. van, Breuning, M.H.

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De novo truncation of chromosome 16p and healing with (TTAGGG)n in the α-thalassemia/mental retardation syndrome (ATR-16) von LAMB, J, HARRIS, P. C, WILKIE, A. O. M, WOOD, W. G, DAUWERSE, J. G, HIGGS, D. R

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A partial BRCA1 sequence homology mapping to 4q28 von Stec, I., van Vliet, M., van Eijk, R., Meijers, H., Kroeze, K.H.G., Dauwerse, J.G., van Ommen, G.-J.B., Cornelisse, C.J., den Dunnen, J.T., Devilee, P.

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Cloning the breakpoint cluster region of the inv(16) in acute nonlymphocytic leukemia M4 Eo von Dauwerse, J.G., Wessels, J.W., Giles, R.H., Wiegant, J., van der Reijden, B.A., Fugazza, G., Jumelet, E.A., Smit, E., Baas, F., Raap, A.K., Hagemeijer, A., Baverstock, G.C., van Ommen, G.J.B., Breuning, M.H.

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A gene for a myosin peptide is disrupted by the inv(16)(p13q22) in acute nonlymphocytic leukemia M4Eo von VAN DER REIJDEN, B. A, DAUWERSE, J. G, WESSELS, J. W, BEVERSTOCK, G. C, HAGEMEIJER, A, VAN OMMEN, G. J. B, BREUNING, M. H

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Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1) von Breuning, M H, Snijdewint, F G, Brunner, H, Verwest, A, Ijdo, J W, Saris, J J, Dauwerse, J G, Blonden, L, Keith, T, Callen, D F

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Reconstruction of the 2.4 Mb human DMD-gene by homologous YAC recombination von DEN DUNNEN, J. T, GROOTSCHOLTEN, P. M, VAN OMMEN, G. J. B, DAUWERSE, J. G, WALKER, A. P, MONACO, A. P, BUTLER, R, ANAND, R, COFFEY, A. J, BENTLEY, D. R, STEENSMA, H. Y

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Lowering of Pkd1 expression is sufficient to cause polycystic kidney disease von Leeuwen, Irma S. Lantinga-van, Dauwerse, Johannes G., Baelde, Hans J., Leonhard, Wouter N., van de Wal, Annemieke, Ward, Christopher J., Verbeek, Sjef, DeRuiter, Marco C., Breuning, Martijn H., de Heer, Emile, Peters, Dorien J.M.

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Three Human Glutamate Dehydrogenase Genes (GLUD1, GLUDP2, and GLUDP3) Are Located on Chromosome 10q, but Are Not Closely Physically Linked von Deloukas, P., Dauwerse, J.G., Moschonas, N.K., van Ommen, G.J.B., van Loon, A.P.G.M.

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Two Distinct Loci on the Short Arm of Chromosome 16 Are Involved in Myeloid Leukemia von Wessels, J.W., Mollevanger, P., Dauwerse, J.G., Cluitmans, F.H.M., Breuning, M.H., Beverstock, G.C.

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Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified... von Driesen, M.S., Dauwerse, J.G., Wapenaar, M.C., Meershoek, E.J., Mollevanger, P., Chen, K.L., Fischbeck, K.H., van Ommen, G.J.B.

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Paternal duplication of chromosome 5q11.2-5q14 in a male born with craniostenosis, ear tags, kidney dysplasia and several other anomalies von BRESLAU-SIDERIUS, E. J, WIJNEN, J. T, DAUWERSE, J. G, DE PATER, J. M, BEEMER, F. A, MEERA KHAN, P

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A TaqI polymorphism identified by 26-6 (D16S125) proximal to the locus affecting adult polycystic kidney disease (PKD1) on chromosome 16 von BREUNING, M. H, SNIJDEWINT, F. G. M, SMITS, J. R, DAUWERSE, J. G, SARIS, J. J, VAN OMMEN, G. J. B

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