Screening for BRCA2 mutations in 81 Dutch breast–ovarian cancer families.

Autor: Peelen, T, Vliet, M van, Bosch, A, Bignell, G, Vasen, H F A, Klijn, J G M, Meijers-Heijboer, H, Stratton, M, Ommen, G-J B van, Cornelisse, C J, Devilee, P

Publikováno v: British Journal of Cancer. 1/1/2000, Vol. 82 Issue 1, p151. 6p.

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e77c1b66697cba59b1266b9edace05f9
https://research.vumc.nl/en/publications/21f059aa-38bd-428a-9b59-47074e11452b

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients (vol 17, pg 341, 1997)

Autor: Petrij-Bosch, A., Peelen, T., van Vliet, M., van Eijk, R., Olmer, R., Drusedau, M., Hogervorst, F. B. L., Hageman, S., Arts, P. J. W., Ligtenberg, M. J. L., Meijers-Heijboer, H., Klijn, J. G. M., Vasen, H. F. A., Cornelisse, C. J., van't Veer, L. J., Bakker, E., van Ommen, G. J., Devilee, P.

Publikováno v: Nature genetics, 17(4). Nature Publishing Group

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=narcis______::0562efd4e401673c7102bd67376070d3
https://pure.amc.nl/en/publications/brca1-genomic-deletions-are-major-founder-mutations-in-dutch-breast-cancer-patients-vol-17-pg-341-1997(8b1fe59f-146d-42c2-b203-5888194e9d38).html

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A Rapid ¹H NMR Assay for Enantiomeric Excess of α-Substituted Aldehydes

Autor: Chi, Y., Peelen, T. J., Gellman, S. H.

Publikováno v: Organic Letters; August 2005, Vol. 7 Issue: 16 p3469-3472, 4p