Research Project:
Kraniofasiyal Malformasyonlara Klinik ve Genetik Yaklaşım

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dc.contributor.departmentSchool of Medicine
dc.contributor.departmentSchool of Medicine
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-12-29T10:38:41Z
dc.date.available2024-12-29
dc.description.publisherscopeNational
dc.identifierTB.00235
dc.identifier.urihttps://hdl.handle.net/20.500.14288/24485
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Projects Collection
dc.relation.relatedpublicationsA novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome
dc.relation.relatedpublicationsFetal skeletal dysplasia cohort of a single tertiary referral center in Istanbul, Turkey
dc.relation.relatedpublicationsALX4 related parietal foramina mimicking encephalocele in prenatal period
dc.relation.relatedpublicationsRevisiting TOP2B-related phenotypes: three new cases and literature review
dc.relation.relatedpublicationsMutations in CDK5RAP2 cause Seckel syndrome
dc.titleKraniofasiyal Malformasyonlara Klinik ve Genetik Yaklaşım
dc.title.alternativeKraniofasiyal Malformasyonlara Klinik
dspace.entity.typeProject
local.contributor.kuauthorKayserili, Hülya
local.project.contractnumber112S398
local.project.endDate2015-10-15
local.project.startDate2012-10-11
local.project.templateTB.ARDEB.UDP.ERANET
project.funder.identifierTÜBİTAK
project.funder.nameTÜBİTAK
project.investigatorKayserili, Hülya
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