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

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dc.contributor.departmentN/A
dc.contributor.departmentN/A
dc.contributor.departmentN/A
dc.contributor.departmentN/A
dc.contributor.departmentN/A
dc.contributor.departmentN/A
dc.contributor.kuauthorSaraçoğlu, Hilal Pırıl
dc.contributor.kuauthorBörklü Yücel, Esra
dc.contributor.kuauthorEraslan, Serpil
dc.contributor.kuauthorYılmaz, Ertürk
dc.contributor.kuauthorAltunoğlu, Umut
dc.contributor.kuauthorKayserili, Hülya
dc.contributor.kuprofilePhD Student
dc.contributor.kuprofileOther
dc.contributor.kuprofileOther
dc.contributor.kuprofileMaster Student
dc.contributor.kuprofileFaculty Member
dc.contributor.kuprofileFaculty Member
dc.contributor.researchcenterKoç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM)
dc.contributor.schoolcollegeinstituteGraduate School of Health Sciences
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.schoolcollegeinstituteGraduate School of Social Sciences and Humanities
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.unitKoç University Hospital
dc.contributor.yokidN/A
dc.contributor.yokidN/A
dc.contributor.yokidN/A
dc.contributor.yokidN/A
dc.contributor.yokid126174
dc.contributor.yokid7945
dc.date.accessioned2024-11-09T22:56:31Z
dc.date.issued2020
dc.description.abstractN/A
dc.description.indexedbyWoS
dc.description.issueSUPPL 1
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.volume28
dc.identifier.doiN/A
dc.identifier.eissn1476-5438
dc.identifier.issn1018-4813
dc.identifier.urihttps://hdl.handle.net/20.500.14288/7380
dc.identifier.wos598482601541
dc.keywordsN/A
dc.languageEnglish
dc.publisherSpringernature
dc.sourceEuropean Journal of Human Genetics
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.authorid0000-0002-3734-489X
local.contributor.authorid0000-0002-1326-0608
local.contributor.authorid0000-0002-7674-7384
local.contributor.authoridN/A
local.contributor.authorid0000-0002-3172-5368
local.contributor.authorid0000-0003-0376-499X
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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