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1
المؤلفون: Blatnik A, Geverink N, Schrock E, Capella G, Vos JR, Balmana J, Lagercrantz SB, Houdayer C, Holinski-Feder E, Claes K, Evans G, Wolkenstein P, Tham E, Ferner RE, Melegh B, Maher E, Woodward E, Hoogerbrugge N, Legius E, Ligtenberg M, Steinke-Lange V, Guillermo IB, Ertmanska K, Hernandez HS, Giepmans L, Krajc M, Vidal JB, Frebourg T, Oostenbrink R, Spier I, Hietala M, on behalf of ERN GENTURIS, Kets M, Lubinski J, Teixeira M, Peltonen S, Bours V, Rohl C, Oliveira C, Lazaro C, Aretz S, Sijmons R, Tischkowitz M, Poppe B
المساهمون: iho- ja sukupuolitautioppi, Dermatology and Venereology, biolääketieteen laitos, yhteiset, Institute of Biomedicine, tyks, vsshp, tyks, vsshp, 2607100, 2607305
العلاقة: 18; Familial Cancer; https://www.utupub.fi/handle/10024/172941Test; URN:NBN:fi-fe2021042827695
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2دورية 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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3دورية أكاديمية
المؤلفون: Genuardi, Maurizio
المساهمون: Sijmons, R, Greenblatt, M, Genuardi, Maurizio
مصطلحات موضوعية: NONPOLYPOSIS COLORECTAL-CANCER, MUTATIONS, CLASSIFICATION, PREDISPOSITION, TUMORS, BRCA1, MODEL, MLH1, Settore MED/03 - GENETICA MEDICA
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23525798; info:eu-repo/semantics/altIdentifier/wos/WOS:000322173700007; volume:12; issue:2; firstpage:181; lastpage:187; issueyear:N/A; journal:FAMILIAL CANCER; http://hdl.handle.net/10807/56966Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84880920383
