Whole Exome Sequencing of consanguineous families of clinically diagnosed with Neurodevelopmental Disorders

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dc.contributor.authorTurkgenc, B.
dc.contributor.authorYararbas, K.
dc.contributor.authorKarakoyun, H. Keskin
dc.contributor.authorYesilyurt, A.
dc.contributor.authorGezdirici, A.
dc.contributor.authorTatli, B.
dc.contributor.authorAkcakaya, N. H.
dc.contributor.authorHacifazlioglu, N. E.
dc.contributor.authorCoskun, O.
dc.contributor.authorYesil, G.
dc.contributor.authorEkici, B.
dc.contributor.authorYildirim, C.
dc.contributor.authorOnal, H.
dc.contributor.authorTuranli, G.
dc.contributor.authorAlanay, Y.
dc.date.accessioned2025-10-16T15:20:14Z
dc.date.issued2020
dc.identifier.otherWOS:000598482603186
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/7487
dc.publisherSPRINGERNATURE
dc.sourceEUROPEAN JOURNAL OF HUMAN GENETICS
dc.titleWhole Exome Sequencing of consanguineous families of clinically diagnosed with Neurodevelopmental Disorders
dc.typeMeeting Abstract

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