Publication:
Lynch syndrome: gene variants in 35 patients and cascade screening of individuals at-risk

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dc.conference.dateJune 6–9, 2020
dc.conference.locationVirtual Conference
dc.conference.organizer53rd European Society of Human Genetics (ESHG) Conference
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.departmentKUH (Koç University Hospital)
dc.contributor.departmentGraduate School of Health Sciences
dc.contributor.departmentSchool of Medicine
dc.contributor.facultymemberYes
dc.contributor.kuauthorAltunoğlu, Umut
dc.contributor.kuauthorBörklü Yücel, Esra
dc.contributor.kuauthorEraslan, Serpil
dc.contributor.kuauthorKayserili, Hülya
dc.contributor.kuauthorSaraçoğlu, Hilal Pırıl
dc.contributor.kuauthorYılmaz, Ertürk
dc.contributor.schoolcollegeinstituteGRADUATE SCHOOL OF HEALTH SCIENCES
dc.contributor.schoolcollegeinstituteKUH (KOÇ UNIVERSITY HOSPITAL)
dc.contributor.schoolcollegeinstituteResearch Center
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T22:56:31Z
dc.date.issued2020
dc.description.abstractBAKILACAK
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.openaccessNO
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.studentonlypublicationNo
dc.description.studentpublicationYes
dc.description.versionN/A
dc.identifier.WoSQuartileQ1
dc.identifier.eissn1476-5438
dc.identifier.embargoN/A
dc.identifier.endpage529
dc.identifier.issn1018-4813
dc.identifier.linkhttps://www.nature.com/articles/s41431-020-00739-z
dc.identifier.startpage529
dc.identifier.urihttps://hdl.handle.net/20.500.14288/7380
dc.identifier.wos000598482601541
dc.language.isoeng
dc.publisherSpringer Nature
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofEuropean Journal of Human Genetics
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectBiochemistry
dc.subjectMolecular biology
dc.subjectGenetics
dc.subjectHeredity
dc.titleLynch syndrome: gene variants in 35 patients and cascade screening of individuals at-risk
dc.typeMeeting Abstract
dspace.entity.typePublication
local.contributor.kuauthorSaraçoğlu, Hilal Pırıl
local.contributor.kuauthorBörklü Yücel, Esra
local.contributor.kuauthorEraslan, Serpil
local.contributor.kuauthorYılmaz, Ertürk
local.contributor.kuauthorAltunoğlu, Umut
local.contributor.kuauthorKayserili, Hülya
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