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Making sense of missense in Lynch syndrome: the clinical perspectiveLynch, Henry T ; Jascur, Thomas ; Lanspa, Stephen ; Boland, C RichardCancer prevention research (Philadelphia, Pa.), 2010-11, Vol.3 (11), p.1371-1374 [Periódico revisado por pares]United StatesTexto completo disponível |
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Material Type: Artigo
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Phenotypic heterogeneity in hereditary non-polyposis colorectal cancer: identical germline mutations associated with variable tumour morphology and immunohistochemical expressionHalvarsson, Britta ; Müller, Wolfram ; Planck, Maria ; Benoni, Anna Clara ; Mangell, Peter ; Ottosson, Johan ; Hallén, Magnus ; Isinger, Anna ; Nilbert, MefJournal of clinical pathology, 2007-07, Vol.60 (7), p.781-786 [Periódico revisado por pares]London: BMJ Publishing Group Ltd and Association of Clinical PathologistsTexto completo disponível |