Yayın:
Application of next generation sequencing in rare disorders

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dc.contributor.authorTemel, S. G.
dc.contributor.buuauthorTEMEL, ŞEHİME GÜLSÜN
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıbbi Genetik Ana Bilim Dalı
dc.contributor.orcid0000-0002-9802-0880
dc.contributor.researcheridAAG-8385-2021
dc.date.accessioned2024-09-27T08:08:06Z
dc.date.available2024-09-27T08:08:06Z
dc.date.issued2019-11-15
dc.descriptionBu çalışma, 11-13, Nisan 2019 tarihlerinde Valencia[İspanya]’da düzenlenen European Biotechnology Congress Kongresi‘nde bildiri olarak sunulmuştur.
dc.identifier.doi10.1016/j.jbiotec.2019.05.309
dc.identifier.endpageS11
dc.identifier.issn0168-1656
dc.identifier.issueSupplement S
dc.identifier.startpageS11
dc.identifier.urihttps://doi.org/10.1016/j.jbiotec.2019.05.309
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0168165619308338?via%3Dihub
dc.identifier.urihttps://hdl.handle.net/11452/45386
dc.identifier.volume305
dc.identifier.wos000491118400036
dc.indexed.wosWOS.SCI
dc.indexed.wosWOS.ISTP
dc.language.isoen
dc.publisherElsevier
dc.relation.journalJournal of Biotechnology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBiotechnology & applied microbiology
dc.titleApplication of next generation sequencing in rare disorders
dc.typeOther
dc.type.subtypeMeeting Abstract
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Genetik Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Histoloji ve Embriyoloji Ana Bilim Dalı
local.indexed.atWOS
relation.isAuthorOfPublicationf513efaa-a54e-4cfa-840f-28e2fbdc001a
relation.isAuthorOfPublication.latestForDiscoveryf513efaa-a54e-4cfa-840f-28e2fbdc001a

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