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Dive into the research topics of 'A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome'. Together they form a unique fingerprint.- Sort by
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Els van Riel, Margreet G E M Ausems, Frans B L Hogervorst, Irma Kluijt, Marielle E. van Gijn, Jeanne van Echtelt, Karen Scheidel-Jacobse, Eric F A M Hennekam, Rein P. Stulp, Yvonne J. Vos, G. Johan A Offerhaus, Fred H. Menko, Johan J P Gille
Research output: Contribution to journal › Article › peer-review