Whole exome sequencing of consanguineous families of clinically diagnosed with neurodevelopmental disorders

dc.contributor.authorTürkgenç, Burcu
dc.contributor.authorYararbaş, Kanay
dc.contributor.authorKeskin Karakoyun, Hilal
dc.contributor.authorYeşilyurt, A.
dc.contributor.authorGezdirici, A.
dc.contributor.authorTatlı, B.
dc.contributor.authorAkçakaya, N. Handan
dc.contributor.authorEldeş Hacıfazlıoğlu, Nilüfer
dc.contributor.authorCoşkun, Olcay
dc.contributor.authorYeşil, Gözde
dc.contributor.authorEkici, Barış
dc.contributor.authorYıldırım, Canan
dc.contributor.authorÖnal, Hasan
dc.contributor.authorTuranlı, Güzide
dc.contributor.authorAlanay, Yasemin
dc.date.accessioned2021-01-21T10:41:07Z
dc.date.available2021-01-21T10:41:07Z
dc.date.issued2020
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı
dc.description.abstract[Abstract Not Available]
dc.identifier.citationTürkgenç, B., Yararbaş, K., Keskin Karakoyun, H., Yeşilyurt, A., Gezdirici, A., Tatlı, B. ... Alanay, Y. (2020). Whole exome sequencing of consanguineous families of clinically diagnosed with neurodevelopmental disorders. European Journal of Human Genetics içinde (886-887. ss.).
dc.identifier.endpage887
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.issueSupplement: 1
dc.identifier.startpage886
dc.identifier.urihttps://hdl.handle.net/20.500.12511/6335
dc.identifier.volume28
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherSpringer Nature
dc.relation.ispartofEuropean Journal of Human Geneticsen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectConsanguineous Families
dc.subjectNeurodevelopmental Disorders
dc.subjectExome Sequencing
dc.titleWhole exome sequencing of consanguineous families of clinically diagnosed with neurodevelopmental disorders
dc.typeConference Object

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