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Identification of Genetic Variation in Patients Suspicious of Lynch Syndrome Using Whole Exome Sequencing

dc.contributor.advisorSjursen, Wenche
dc.contributor.advisorDrabløs, Finn
dc.contributor.authorRosnes, Kristine
dc.date.accessioned2021-09-25T16:34:14Z
dc.date.available2021-09-25T16:34:14Z
dc.date.issued2021
dc.identifierno.ntnu:inspera:77744542:27831849
dc.identifier.urihttps://hdl.handle.net/11250/2783290
dc.descriptionFull text available on 2024-01-31
dc.languageeng
dc.publisherNTNU
dc.titleIdentification of Genetic Variation in Patients Suspicious of Lynch Syndrome Using Whole Exome Sequencing
dc.typeMaster thesis


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