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Oculo-auricular syndrome in a new multiplex family does not link to HMX1 or its downstream enhancer

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dc.contributor.coauthorBertoli-Avella, Aida
dc.contributor.kuauthorAltunoğlu, Umut
dc.contributor.kuauthorKaya, Mert
dc.contributor.kuauthorSatkın, Nihan Bilge
dc.contributor.kuauthorBörklü Yücel, Esra
dc.contributor.schoolcollegeinstituteGraduate School of Health Sciences
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.unitKoç University Hospital
dc.date.accessioned2024-12-29T09:37:21Z
dc.date.issued2024
dc.description.indexedbyWoS
dc.description.issueSupplement 1
dc.description.publisherscopeInternational
dc.description.volume32
dc.identifier.eissn1476-5438
dc.identifier.issn1018-4813
dc.identifier.quartileQ2
dc.identifier.urihttps://hdl.handle.net/20.500.14288/22336
dc.identifier.wos1147414901091
dc.keywordsBiochemistry and molecular biology
dc.keywordsGenetics and heredity
dc.languageen
dc.publisherSpringernature
dc.sourceEuropean Journal of Human Genetics
dc.subjectMedicine
dc.titleOculo-auricular syndrome in a new multiplex family does not link to HMX1 or its downstream enhancer
dc.typeMeeting abstract
dspace.entity.typePublication
local.contributor.kuauthorAltunoğlu, Umut
local.contributor.kuauthorKaya, Mert
local.contributor.kuauthorSatkın, Nihan Bilge
local.contributor.kuauthorBörklü Yücel, Esra

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