Impact of deep phenotyping: high diagnostic yield in a diverse pediatric population of 172 patients through clinical whole-genome sequencing at a single center

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dc.contributor.authorAkgun\\-Dogan, Ozlem
dc.contributor.authorBengur, Ecenur Tuc
dc.contributor.authorAy, Beril
dc.contributor.authorOzkose, Gulsah Sebnem
dc.contributor.authorKar, Emre
dc.contributor.authorBengur, Fuat Baris
dc.contributor.authorBulut, Aybike S.
dc.contributor.authorYigit, Ayca
dc.contributor.authorAydin, Eylul
dc.contributor.authorEsen, Fatma Nisa
dc.contributor.authorOzdemir, Ozkan
dc.contributor.authorYesilyurt, Ahmet
dc.contributor.authorAlanay, Yasemin
dc.date.accessioned2025-10-16T15:13:38Z
dc.date.issued2024
dc.identifier.doi10.3389/fgene.2024.1347474
dc.identifier.otherWOS:001193119300001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5891
dc.publisherFRONTIERS MEDIA SA
dc.sourceFRONTIERS IN GENETICS
dc.subjectwhole\\-genome sequencing
dc.subjectfirst tier
dc.subjectdiagnostic yield
dc.subjectundiagnosed patients
dc.subjectpediatric geneticist
dc.titleImpact of deep phenotyping: high diagnostic yield in a diverse pediatric population of 172 patients through clinical whole-genome sequencing at a single center
dc.typeArticle

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