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61دورية أكاديمية
المؤلفون: Harinck, F, Konings, I C A W, Kluijt, I, Poley, J W, van Hooft, J E, van Dullemen, H M, Nio, C Y, Krak, N C, Hermans, J J, Aalfs, C M, Wagner, A, Sijmons, R H, Biermann, K, van Eijck, C H, Gouma, D J, Dijkgraaf, M G W, Fockens, P, Bruno, M J
المصدر: Gut ; volume 65, issue 9, page 1505-1513 ; ISSN 0017-5749 1468-3288
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المساهمون: Guided Treatment in Optimal Selected Cancer Patients (GUTS), Targeted Gynaecologic Oncology (TARGON), Damage and Repair in Cancer Development and Cancer Treatment (DARE)
المصدر: International Journal of Behavioral Medicine, 21, S49-S49. SPRINGER
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=narcis______::62cb5e519e3680d767fcd96c14d1a7faTest
https://research.rug.nl/en/publications/d3000463-9966-442d-a248-ce2289f818f4Test -
63دورية أكاديمية
المؤلفون: Leung, SY, Bernstein, I, Thompson, BA, Spurdle, AB, Plazzer, JP, Greenblatt, MS, Akagi, K, Al-Mulla, F, Bapat, B, 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, 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, on behalf of, INSIGHT
العلاقة: Nature Genetics; Nature Genetics, 2014, v. 46 n. 2, p. 107–115; 107–115; 227453; WOS:000331208300006; http://hdl.handle.net/10722/193930Test; 46
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64دورية أكاديمية
المؤلفون: Ferronika, P., Bergsma, J., Li, J., Terpstra, M. M., Lelieveld-Kors, A. M., Danarto, R., Sijmons, R. H., Kats-Ugurlu, G., Moeljono, A., Kok, K.
المصدر: Ferronika , P , Bergsma , J , Li , J , Terpstra , M M , Lelieveld-Kors , A M , Danarto , R , Sijmons , R H , Kats-Ugurlu , G , Moeljono , A & Kok , K 2014 , ' Paraffin embedded tissue as valuable and challenging resource for studying intratumoral genetic heterogeneity of clear cell renal cell carcinoma ' , European Journal of Cancer , vol. 50 , pp. S78 .
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65دورية أكاديمية
المؤلفون: Van Den Berg-De Ruiter, E., van Min, M., Mulder, A., Vellenga, E., Splinter, E., de Wit, E., Klous, P., van der Vlies, P., Weening, D., van Diemen, C., Sijmons, R., Sinke, R., Raddatz, B.
المصدر: Van Den Berg-De Ruiter , E , van Min , M , Mulder , A , Vellenga , E , Splinter , E , de Wit , E , Klous , P , van der Vlies , P , Weening , D , van Diemen , C , Sijmons , R , Sinke , R & Raddatz , B 2014 , ' A comprehensive new DNA test for detection of fusion genes in leukemia ' , Haematologica , vol. 99 , pp. 276-276 .
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66دورية أكاديمية
المؤلفون: Plazzer, J. P., Sijmons, R. H., Woods, M. O., Peltomaki, P., Thompson, B., Den Dunnen, J. T., Macrae, F.
مصطلحات موضوعية: Lynch Syndrome, InSiGHT database, Microattribution, Variant interpretation, Variant classification, 1306 Cancer Research, 1311 Genetics, 2716 Genetics (clinical), 2730 Oncology
العلاقة: Not set
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67دورية أكاديمية
المصدر: Helder-Woolderink , J M , De Bock , G H , Sijmons , R H , Hollema , H & Mourits , M J E 2013 , ' The additional value of endometrial sampling in the early detection of endometrial cancer in women with Lynch syndrome ' , Gynecologic Oncology , vol. 131 , no. 2 , pp. 304-308 . https://doi.org/10.1016/j.ygyno.2013.05.032Test
مصطلحات موضوعية: Lynch syndrome, Endometrial cancer, Gynecological screening, Premalignancy, Microcurettage, HNPCC, NONPOLYPOSIS COLORECTAL-CANCER, GYNECOLOGIC CANCERS, SURVEILLANCE, RISK, ULTRASOUND, CARCINOMA, MUTATIONS
الإتاحة: https://doi.org/10.1016/j.ygyno.2013.05.032Test
https://hdl.handle.net/11370/0b0518f1-7a21-45b1-aca6-9c2e790b7393Test
https://research.rug.nl/en/publications/0b0518f1-7a21-45b1-aca6-9c2e790b7393Test -
68دورية أكاديمية
المؤلفون: Plazzer, J. P., Sijmons, R. H., Woods, M. O., Peltomaki, P., Thompson, B., Den Dunnen, J. T., Macrae, F.
المصدر: Plazzer , J P , Sijmons , R H , Woods , M O , Peltomaki , P , Thompson , B , Den Dunnen , J T & Macrae , F 2013 , ' The InSiGHT database : utilizing 100 years of insights into Lynch Syndrome ' , Familial Cancer , vol. 12 , no. 2 , pp. 175-180 . https://doi.org/10.1007/s10689-013-9616-0Test
مصطلحات موضوعية: Lynch Syndrome, InSiGHT database, Microattribution, Variant interpretation, Variant classification
الإتاحة: https://doi.org/10.1007/s10689-013-9616-0Test
https://hdl.handle.net/11370/24889aff-91a2-42a5-bcc4-552a40be1e62Test
https://research.rug.nl/en/publications/24889aff-91a2-42a5-bcc4-552a40be1e62Test -
69كتاب
المؤلفون: Lutke Holzik, M. F., Sonneveld, D. J. A., Hoekstra, H. J., Nolte, I. M., Bruinenberg, M., van der Graaf, W. T. A., Sleijfer, D. Th., Sijmons, R. H., Buys, C. H. C. M., Te Meerman, G. J.
المصدر: Germ Cell Tumours V ; page 45-46 ; ISBN 9781447132837 9781447132813
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70دورية أكاديمية
المؤلفون: de Leeuw, N., Dijkhuizen, T., Hehir-Kwa, J., Carter, N., Feuk, L., Firth, H., Kuhn, R., Ledbetter, D., Martin, C., van Ravenswaaij-Arts, C., Scherer, S., Shams, S., Van Vooren, S., Sijmons, R., Swertz, M., Hastings, R.
المصدر: Human Mutation, 33, pp. 930-940
مصطلحات موضوعية: NCMLS 6: Genetics and epigenetic pathways of disease IGMD 3: Genomic disorders and inherited multi-system disorders
