P9 (DXYS75) detects a VNTR-type RFLP in the pseudoautosomal region

Por Wapenaar, M.C., Pearson, P.L., Van Ommen, G.J.B.
Publicado em 1990

An alternative to FISH: detecting deletion and duplication carriers within 24 hours

Por White, S, Sterrenburg, E, van Ommen, G-J B, den Dunnen, J T, Breuning, M
Publicado em 2003

Behavioural complaints in participants who underwent predictive testing for Huntington's disease

Por Witjes-Ane, M, Zwinderman, A, Tibben, A, van Ommen, G-J B, Roos, R
Publicado em 2002

Fluorescent labelling of cRNA for microarray applications

Por ’t Hoen, Peter A. C., de Kort, Floor, van Ommen, G. J. B., den Dunnen, Johan T.
Publicado em 2003

Probe 218EP6 (D16S246) detects RFLP's close to the locus affecting adult polycystic kidney disease (PKD1) on chromosome 16

Por Snijdewint, F.G.M., Saris, J.J., Dauwerse, J.G., Breuning, M.H., Van Ommen, G.J.B.
Publicado em 1990

A TaqI polymorphism identified by 26-6 (D16S125) proximal to the locus affecting adult polycystic kidney disease (PKD1) on chromosome 16

Por Breuning, M.H., Snijdewint, F.G.M., Smits, J.R., Dauwerse, J.G., Saris, J.J., Van Ommen, G.J.B.
Publicado em 1990

Genomic imbalances in mental retardation

Por Kriek, M, White, S, Bouma, M, Dauwerse, H, Hansson, K, Nijhuis, J, Bakker, B, van Ommen, G-J B, den Dunnen, J T, Breuning, M
Publicado em 2004

DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type)

Por Bakker, E., van Broeckhoven, C., Haan, J., Voorhoeve, E., van Hul, W., Levy, E., Lieberburg, I., Carman, M. D., van Ommen, G. J. B., Frangione, B., Roos, R. A. C.
Publicado em 1991

Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter

Por Wijmenga, C., Sandkuijl, L. A., Moerer, P., van der Boorn, N., Bodrug, S. E., Ray, P. N., Brouwer, O. F., Murray, J. C., van Ommen, G. J. B., Padberg, G. W., Frants, R. R.
Publicado em 1992

Deleterious Alleles in the Human Genome Are on Average Younger Than Neutral Alleles of the Same Frequency

Por Kiezun, Adam, Pulit, Sara L., Francioli, Laurent C., van Dijk, Freerk, Swertz, Morris, Boomsma, Dorret I., van Duijn, Cornelia M., Slagboom, P. Eline, van Ommen, G. J. B., Wijmenga, Cisca, de Bakker, Paul I. W., Sunyaev, Shamil R.
Publicado em 2013

Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations

Por Petrij, F., Dauwerse, H., Blough, R., Giles, R., van der Smagt, J. J, Wallerstein, R., Maaswinkel-Mooy, P., van Karnebeek, C. D, van Ommen, G.-J. B, van Haeringen, A., Rubinstein, J., Saal, H., Hennekam, R., Peters, D., Breuning, M.
Publicado em 2000

The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion

Por Koenig, M., Beggs, A. H., Moyer, M., Scherpf, S., Heindrich, K., Bettecken, T., Meng, G., Müller, C. R., Lindlöf, M., Kaariainen, H., de la Chapelle, A., Kiuru, A., Savontaus, M.-L., Gilgenkrantz, H., Récan, D., Chelly, J., Kaplan, J.-C., Covone, A. E., Archidiacono, N., Romeo, G., Liechti-Gallati, S., Schneider, V., Braga, S., Moser, H., Darras, B. T., Murphy, P., Francke, U., Chen, J. D., Morgan, G., Denton, M., Greenberg, C. R., Wrogemann, K., Blonden, L. A. J., van Paassen, H. M. B., van Ommen, G. J. B., Kunkel, L. M.
Publicado em 1989

A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

Por Peelen, T., van Vliet, M., Petrij-Bosch, A., Mieremet, R., Szabo, C., van den Ouweland, A. M. W., Hogervorst, F., Brohet, R., Ligtenberg, M. J. L., Teugels, E., van der Luijt, R., van der Hout, A. H., Gille, J. J. P., Pals, G., Jedema, I., Olmer, R., van Leeuwen, I., Newman, B., Plandsoen, M., van der Est, M., Brink, G., Hageman, S., Arts, P. J. W., Bakker, M. M., Willems, H. W., van der Looij, E., Neyns, B., Bonduelle, M., Jansen, R., Oosterwijk, J. C., Sijmons, R., Smeets, H. J. M., van Asperen, C. J., Meijers-Heijboer, H., Klijn, J. G. M., de Greve, J., King, M.-C., Menko, F. H., Brunner, H. G., Halley, D., van Ommen, G.-J. B., Vasen, H. F. A., Cornelisse, C. J., van 'tVeer, L. J., de Knijff, P., Bakker, E., Devilee, P.
Publicado em 1997