Isolation of a candidate gene for Norrie disease by positional cloning
Berger, W, Meindl, A, van de Pol, T.J.R, Cremers, F.P.M, Ropers, H.H, Döerner, C, Monaco, A, Bergen, A.A.B, Lebo, R, Warburg, M, Zergollern, L, Lorenz, B, Gal, A, Bleeker-Wagemakers, E.M, Meitinger, T
Published in Nature genetics (01.06.1992)
Published in Nature genetics (01.06.1992)
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On the many faces of Leber hereditary optic neuropathy
Oostra, R.J., Tijmes, N.T., Cobben, J.M., Boihuis, P.A., van Nesselrooij, B.P.M., Houtman, W.A., de Kok-Nazaruk, M.M., Bleeker-Wagemakers, E.M.
Published in Clinical genetics (01.06.1997)
Published in Clinical genetics (01.06.1997)
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Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?
Moog, U, Bleeker-Wagemakers, E M, Crobach, P, Vles, J S, Schrander-Stumpel, C T
Published in American journal of medical genetics (07.07.1998)
Published in American journal of medical genetics (07.07.1998)
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3233 Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome IQ; exclusion of the phosducin gene
van Soest, S., Te Nijenhuis, S., van den Born, L.I., Bleeker-Wagemakers, E.M., Sankuul, L.A., Westerveld, A., Bergen, A.A.B.
Published in Vision research (Oxford) (01.10.1995)
Published in Vision research (Oxford) (01.10.1995)
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P 376 Phenotypical and genotypical classification of autosomal recessive RP
Van den Born, L.I., Van Soest, S., Riemslag, F.C.C., Bergen, A.A.B., Bleeker-Wagemakers, E.M., De Jong, P.T.V.M.
Published in Vision research (Oxford) (01.10.1995)
Published in Vision research (Oxford) (01.10.1995)
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Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy
Bolhuis, P.A., Bleeker-Wagemakers, E.M., Ponne, N.J., Van Schooneveld, M.J., Westerveld, A., Van den Bogert, C., Tabak, H.F.
Published in Biochemical and biophysical research communications (16.08.1990)
Published in Biochemical and biophysical research communications (16.08.1990)
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Integrated genetic and physical map of the 1q31 → q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenes
VAN SOEST, S, VAN ROSSEM, M. J, HECKENLIVELY, J. R, VAN DEN BORN, L. I, DE MEULEMEESTER, T. M. A. M. O, VLIEX, S, DE JONG, P. T. V. M, BLEEKER-WAGEMAKERS, E. M, WESTERVELD, A, BERGEN, A. A. B
Published in Cytogenetic and genome research (1999)
Published in Cytogenetic and genome research (1999)
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Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q ; exclusion of the phosducin gene (PDC)
VAN SOEST, S, TE NIJENHUIS, S, VAN DEN BORN, L. I, BLEEKER-WAGEMAKERS, E. M, SHARP, E, SANDKUIJL, L. A, WESTERVELD, A, BERGEN, A. A. B
Published in Cytogenetic and genome research (01.01.1996)
Published in Cytogenetic and genome research (01.01.1996)
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Journal Article
The distal region of 11p13 and associated genetic diseases
Mannens, M., Hoovers, J.M.N., Bleeker-Wagemakers, E.M., Redeker, E., Bliek, J., Overbeeke-Melkert, M., Saunders, G., Williams, B., van Heynigen, V., Junien, C., Haber, D., Speleman, F., Heyting, C., Slater, R.M., Leschot, N.J., Westerveld, A.
Published in Genomics (San Diego, Calif.) (01.10.1991)
Published in Genomics (San Diego, Calif.) (01.10.1991)
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Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloning
Bergen, A A, Wapenaar, M C, Schuurman, E J, Diergaarde, P J, Lerach, H, Monaco, A P, Bakker, E, Bleeker-Wagemakers, E M, van Ommen, G J
Published in Cytogenetics and cell genetics (01.01.1993)
Published in Cytogenetics and cell genetics (01.01.1993)
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Physical fine-mapping of a deletion spanning the Norrie gene
Diergaarde, P J, Wieringa, B, Bleeker-Wagemakers, E M, Sims, K B, Breakefield, X O, Ropers, H H
Published in Human genetics (01.12.1989)
Published in Human genetics (01.12.1989)
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Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family
Mannens, M, Bleeker-Wagemakers, E M, Bliek, J, Hoovers, J, Mandjes, I, van Tol, S, Frants, R R, Heyting, C, Westerveld, A, Slater, R M
Published in Cytogenetics and cell genetics (01.01.1989)
Published in Cytogenetics and cell genetics (01.01.1989)
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Congenital Eversion of the Eyelids in a Case of Down's Syndrome
Bleeker-Wagemakers, E.M., Delleman, J.W., van Walbeek, K.
Published in Ophthalmologica (Basel) (01.01.1976)
Published in Ophthalmologica (Basel) (01.01.1976)
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