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Whole exome sequencing in fetal structural abnormalities: experience of 8 cases

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dc.contributor.coauthorAltunoğlu, Umut
dc.contributor.coauthorKalaycı, Tuğba
dc.contributor.coauthorKalelioğlu, İbrahim Halil
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorKayserili, Hülya
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:42:19Z
dc.date.issued2018
dc.description.indexedbyWOS
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume26
dc.identifier.eissn1476-5438
dc.identifier.issn1018-4813
dc.identifier.quartileQ1
dc.identifier.urihttps://hdl.handle.net/20.500.14288/13293
dc.identifier.wos489312601106
dc.keywordsBiochemistry and molecular biology
dc.keywordsGenetics and heredity
dc.language.isoeng
dc.publisherNature Publishing Group
dc.relation.ispartofEuropean Journal of Human Genetics
dc.subjectBiochemistry
dc.subjectMolecular biology
dc.subjectGenetics
dc.subjectHeredity
dc.titleWhole exome sequencing in fetal structural abnormalities: experience of 8 cases
dc.typeMeeting Abstract
dspace.entity.typePublication
local.contributor.kuauthorKayserili, Hülya
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
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relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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