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1مؤتمر
المؤلفون: Plantinga, M., Van Langen, I., Ranchor, A., Lanting, P., Wilffert, B., Sijmons, R.
المصدر: Plantinga , M , Van Langen , I , Ranchor , A , Lanting , P , Wilffert , B & Sijmons , R 2019 , ' Personalized medicine via Pharmacogenetics: Investigating critical success factors for clinical implementation ' , pp. 692 . https://doi.org/10.1038/s41431-018-0247-7Test
مصطلحات موضوعية: adult, case report, clinical article, conference abstract, decision support system, female, geriatrics, human, internal medicine, interview, male, personalized medicine, pharmacist, pharmacogenetics, psychiatry, responsibility, software, university hospital
الإتاحة: https://doi.org/10.1038/s41431-018-0247-7Test
https://hdl.handle.net/11370/b8da3e65-eb7c-44f0-9095-cb1af312080cTest
https://research.rug.nl/en/publications/b8da3e65-eb7c-44f0-9095-cb1af312080cTest -
2دورية أكاديمية
المؤلفون: Thompson, Ba, Spurdle, Ab, Plazzer, Jp, Greenblatt, Ms, Akagi, K, Al Mulla, F, Bapat, B, Bernstein, I, Capellá, G, den Dunnen, Jt, du Sart, D, Fabre, A, Farrell, Mp, Farrington, Sm, Frayling, Im, Frebourg, T, Goldgar, De, Heinen, Cd, Holinski Feder, E, Kohonen Corish, M, Robinson, Kl, Leung, Sy, Martins, A, Moller, P, Morak, M, Nystrom, M, Peltomaki, P, Pineda, M, Qi, M, Ramesar, R, Rasmussen, Lj, Royer Pokora, B, Scott, Rj, Sijmons, R, Tavtigian, Sv, Tops, Cm, Weber, T, Wijnen, J, Woods, Mo, Macrae, F, Genuardi, M, PEDRONI, Monica
المساهمون: Thompson, Ba, Spurdle, Ab, Plazzer, Jp, Greenblatt, M, Akagi, K, Al Mulla, F, Bapat, B, Bernstein, I, Capellá, G, den Dunnen, Jt, du Sart, D, Fabre, A, Farrell, Mp, Farrington, Sm, Frayling, Im, Frebourg, T, Goldgar, De, Heinen, Cd, Holinski Feder, E, Kohonen Corish, M, Robinson, Kl, Leung, Sy, Martins, A, Moller, P, Morak, M, Nystrom, M, Peltomaki, P, Pineda, M, Qi, M, Ramesar, R, Rasmussen, Lj, Royer Pokora, B, Scott, Rj, Sijmons, R, Tavtigian, Sv, Tops, Cm, Weber, T, Wijnen, J, Woods, Mo, Macrae, F, Genuardi, M, Pedroni, Monica
مصطلحات موضوعية: Classification, DNA Mismatch Repair, Disease Management, Gastrointestinal Neoplasm, Genetic Variation, Human, Databases, Genetic
وصف الملف: ELETTRONICO
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/24362816; info:eu-repo/semantics/altIdentifier/wos/WOS:000331208300006; volume:46; firstpage:107; lastpage:115; journal:NATURE GENETICS; http://hdl.handle.net/11380/1062794Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84895789502
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3دورية أكاديمية
المؤلفون: Nelen, M R, van Staveren, W C, Peeters, E A, Hassel, M B, Gorlin, R J, Hamm, H, Lindboe, C F, Fryns, Jean-Pierre, Sijmons, R H, Woods, D G, Mariman, E C, Padberg, G W, Kremer, H
مصطلحات موضوعية: Adult, Chromosome Mapping, Chromosomes, Human, Pair 10, DNA Mutational Analysis, Female, Genes, Tumor Suppressor, Germ-Line Mutation, Hamartoma Syndrome, Multiple, Humans, Male, PTEN Phosphohydrolase, Pedigree, Phosphoric Monoester Hydrolases, Protein Tyrosine Phosphatases, Tumor Suppressor Proteins
العلاقة: Human molecular genetics vol:6 issue:8 pages:1383-7; https://lirias.kuleuven.be/handle/123456789/283226Test; http://hmg.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=9259288Test
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4دورية أكاديمية
المؤلفون: 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 't Ver, L. J., de Knijff, P., Bakker, E., Devilee, P.
المصدر: The American Journal of Human Genetics, 60(5)
مصطلحات موضوعية: Founder effect, Mammary gland diseases, Ovaire, Homme, Etude familiale, Female, Human, Mutation, Glande mammaire, Belgium, Family study, Ovary, Effet fondateur, Malignant tumor, Femelle, Tumeur maligne, Female genital diseases, Molecular biology, Genetic inheritance, Mammary gland, Europe, Netherlands
العلاقة: https://doi.org/10.17615/jkkh-v976Test; https://cdr.lib.unc.edu/downloads/hh63t416f?file=thumbnailTest; https://cdr.lib.unc.edu/downloads/hh63t416fTest
الإتاحة: https://doi.org/10.17615/jkkh-v976Test
https://cdr.lib.unc.edu/downloads/hh63t416f?file=thumbnailTest
https://cdr.lib.unc.edu/downloads/hh63t416fTest -
5دورية أكاديمية
المؤلفون: Oosterwijk, J C, Sijmons, R H, Menko, F H, Chorus, A M, Rookus, M A
المصدر: Oosterwijk , J C , Sijmons , R H , Menko , F H , Chorus , A M & Rookus , M A 1995 , ' De kans op mammacarcinoom en samenhangende carcinomen bij een positieve familieanamnese. Landelijke Werkgroep Erfelijk Mammacarcinoom van de Stichting Opsporing Erfelijke Tumoren ' , Nederlands Tijdschrift voor de Geneeskunde , vol. 139 , no. 9 , pp. 423-8 .
مصطلحات موضوعية: Adult, Aged, Breast Neoplasms, Male, Chromosomes, Human, Pair 13, Pair 17, DNA, Neoplasm, Female, Genetic Counseling, Genetic Markers, Humans, Middle Aged, Ovarian Neoplasms, Risk Assessment, Risk Factors