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dc.contributor.authorHoulleberghs, H.J.L.en_US
dc.date.accessioned2018-07-30T05:50:14Z
dc.date.available2018-07-30T05:50:14Z
dc.date.issued2017-01-30en_US
dc.identifier.urihttp://hdl.handle.net/1871/55045
dc.description.sponsorshipRiele, H.P.J. te [Promotor]en_US
dc.description.sponsorshipVerhoef, S. [Copromotor]en_US
dc.format.extent167 pen_US
dc.language.isoenen_US
dc.publisherAmsterdam: Vrije Universiteiten_US
dc.subjectMismatch repairen_US
dc.subjectLynch syndromeen_US
dc.subjectMSH2en_US
dc.subjectMSH6en_US
dc.subjectMLH1en_US
dc.subjectunclassified variantsen_US
dc.subjectoligonucleotide-directed mutation screenen_US
dc.titleOligonucleotide-directed mutation screening: a functional test to classify mismatch repair gene variants of uncertain significanceen_US
dc.typeDoctoral thesisen_US


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