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

Autor: Peelen, T, van Vliet, M, Petrij-Bosch, A, Mieremet, R, Szabo, C, van den Ouweland, A M, Hogervorst, F, Brohet, R, Ligtenberg, M J, Teugels, E, van der Luijt, R, van der Hout, A H, Gille, J J, Pals, G, Jedema, I, Olmer, R, van Leeuwen, I, Newman, B, Plandsoen, M, van der Est, M, Brink, G, Hageman, S, Arts, P J, Bakker, M M, Devilee, P

Publikováno v: Peelen, T, van Vliet, M, Petrij-Bosch, A, Mieremet, R, Szabo, C, van den Ouweland, A M, Hogervorst, F, Brohet, R, Ligtenberg, M J, Teugels, E, van der Luijt, R, van der Hout, A H, Gille, J J, Pals, G, Jedema, I, Olmer, R, van Leeuwen, I, Newman, B, Plandsoen, M, van der Est, M, Brink, G, Hageman, S, Arts, P J, Bakker, M M & Devilee, P 1997, ' A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families ', American journal of human genetics, vol. 60, no. 5, pp. 1041-9 .
American journal of human genetics, 60(5), 1041-9. Cell Press

We have identified 79 mutations in BRCA1 in a set of 643 Dutch and 23 Belgian hereditary breast and ovarian cancer families collected either for research or for clinical diagnostic purposes. Twenty-eight distinct mutations have been observed, 18 of t

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Publikováno v: Gut; Nov1991, Vol. 32 Issue 11, p1291-1294, 4p, 1 Chart, 2 Graphs

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

Autor: Peelen T; Department of Human Genetics, Leiden University Medical Center, The Netherlands., van Vliet M, Petrij-Bosch A, Mieremet R, Szabo C, van den Ouweland AM, Hogervorst F, Brohet R, Ligtenberg MJ, Teugels E, van der Luijt R, van der Hout AH, Gille JJ, Pals G, Jedema I, Olmer R, van Leeuwen I, Newman B, Plandsoen M, van der Est M, Brink G, Hageman S, Arts PJ, Bakker MM, Devilee P, et. al.

Publikováno v: American journal of human genetics [Am J Hum Genet] 1997 May; Vol. 60 (5), pp. 1041-9.

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Autor: van den Ouweland AM; Department of Clinical Genetics, Erasmus University, Rotterdam, The Netherlands., van der Est MN, Wesby-van Swaay E, Tijmensen TS, Los FJ, Van Hemel JO, Hennekam RC, Meijers-Heijboer HJ, Niermeijer MF, Halley DJ

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