Cleidocranialdysplasia. Amolecularandclinicalreview

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dc.contributor.authorFortunato, Leonzio
dc.contributor.authorYavuz, İzzet
dc.contributor.authorPlotino, Gianluca
dc.contributor.authorAvendano, Andrea
dc.contributor.authorCallea, Michele
dc.contributor.authorGrande, Nicola Maria
dc.contributor.authorRizal, Mochamad Fahlevi
dc.date.accessioned2024-04-24T19:11:21Z
dc.date.available2024-04-24T19:11:21Z
dc.date.issued2018
dc.departmentDicle Üniversitesien_US
dc.description.abstractCleidocranial dysplasia (CCD) is a rare autosomal dominant disorder characterized by skeletal and dental abnormalities primarily, short stature, aplasia or hypoplasia of clavicles, open fontanelles and supernumerary teeth. Heterozygous mutations of the runt-related transcription factor 2 (RUNX2) gene have been found in approximately 60-70% of cases,leaving a large number of cases with no defined genetic cause which ledus to delve into molecular mechanisms underlying CCD and thus to detect potential target genes to be explored in these patients. In this review,we also highlight very broadly the phenotypic characteristics of previously reported patients with CCD.en_US
dc.identifier.doi10.5577/intdentres.2018.vol8.no1.6
dc.identifier.endpage38en_US
dc.identifier.issn2146-1767
dc.identifier.issue1en_US
dc.identifier.startpage35en_US
dc.identifier.trdizinid367125
dc.identifier.urihttps://doi.org/10.5577/intdentres.2018.vol8.no1.6
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/367125
dc.identifier.urihttps://hdl.handle.net/11468/27944
dc.identifier.volume8en_US
dc.indekslendigikaynakTR-Dizin
dc.language.isoenen_US
dc.relation.ispartofInternational Dental Research
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleCleidocranialdysplasia. Amolecularandclinicalreviewen_US
dc.titleCleidocranialdysplasia. Amolecularandclinicalreview
dc.typeOtheren_US

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