Mutations in the candidate gene for Norrie disease by Berger, Wolfgang, de Pol, Dorien van, Warburg, Mette, Gal, Andreas, Bleeker-Wagemakers, Liesbeth, de Silva, Harendra, Meindl, Alfons, Meitinger, Thomas, Cremers, Frans, Ropers, Hans-Hilger

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Positional Cloning of the Gene for X-Linked Retinitis Pigmentosa 3: Homology with the Guanine-Nucleotide-Exchange Factor RCC1 by Roepman, Ronald, van Duijnhoven, Gerard, Rosenberg, Thomas, Pinckers, Alfred J. L. G., Bleeker-Wagemakers, Liesbeth M., Bergen, Arthur A. B., Post, Jan, Beck, Alfred, Reinhardt, Richard, Ropers, Hans-Hilger, Cremers, Frans P. M., Berger, Wolfgang

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Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes by Lenders, J W, Eisenhofer, G, Abeling, N G, Berger, W, Murphy, D L, Konings, C H, Wagemakers, L M, Kopin, I J, Karoum, F, van Gennip, A H, Brunner, H G

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Refinement of the chromosomal position of the X linked juvenile retinoschisis gene by Bergen, A A, ten Brink, J B, Bleeker-Wagemakers, L M, van Schooneveld, M J

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Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp by GAL, A, SCHINZEL, A, ORTH, U, FRASER, N. A, MOLLICA, F, CRAIG, I. W, KRUSE, T, MÄCHLER, M, NEUGEBAUER, M, BLEEKER-WAGEMAKERS, L. M

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Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome by BLEEKER-WAGEMAKERS, L. M, FRIEDRICH, U, GAL, A, WIENKER, T. F, WARBURG, M, ROPERS, H.-H

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Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome by Bijlsma, J B, de France, H F, Bleeker-Wagemakers, L M, Dijkstra, P F

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