Identification of Genetic Variation in Patients Suspicious of Lynch Syndrome Using Whole Exome Sequencing
dc.contributor.advisor | Sjursen, Wenche | |
dc.contributor.advisor | Drabløs, Finn | |
dc.contributor.author | Rosnes, Kristine | |
dc.date.accessioned | 2021-09-25T16:34:14Z | |
dc.date.available | 2021-09-25T16:34:14Z | |
dc.date.issued | 2021 | |
dc.identifier | no.ntnu:inspera:77744542:27831849 | |
dc.identifier.uri | https://hdl.handle.net/11250/2783290 | |
dc.description | Full text available on 2024-01-31 | |
dc.language | eng | |
dc.publisher | NTNU | |
dc.title | Identification of Genetic Variation in Patients Suspicious of Lynch Syndrome Using Whole Exome Sequencing | |
dc.type | Master thesis |
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