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FGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia

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dc.contributor.authorsTurkyilmaz, A.; Geckinli, B. B.; Ates, E. Arslan; Soylemez, M. A.; Guney, A. I.; Ata, P.; Arman, A.
dc.date.accessioned2022-03-12T16:24:07Z
dc.date.accessioned2026-01-11T06:02:54Z
dc.date.available2022-03-12T16:24:07Z
dc.date.issued2019
dc.identifier.doidoiWOS:000489313107050
dc.identifier.eissn1476-5438
dc.identifier.issn1018-4813
dc.identifier.urihttps://hdl.handle.net/11424/226223
dc.identifier.wosWOS:000489313107050
dc.language.isoeng
dc.publisherNATURE PUBLISHING GROUP
dc.relation.ispartofEUROPEAN JOURNAL OF HUMAN GENETICS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleFGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia
dc.typeconferenceObject
dspace.entity.typePublication
oaire.citation.endPage893
oaire.citation.startPage893
oaire.citation.titleEUROPEAN JOURNAL OF HUMAN GENETICS
oaire.citation.volume27

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