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.authorDogan, Ozlem Akgun
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
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.accessioned2025-10-16T15:12:21Z
dc.date.issued2024
dc.description.abstract57th Conference of the European-Society-of-Human-Genetics (ESHG), Berlin, GERMANY, JUN 01-04, 2024
dc.identifier.otherWOS:001407868902445
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5391
dc.publisherSPRINGERNATURE
dc.sourceEUROPEAN JOURNAL OF HUMAN GENETICS
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.typeMeeting Abstract

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