Deletion of macro domain containing 2(MACRO D2) associated with transient hydrops fetalis

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dc.contributor.authorCilingir, I. Uzun
dc.contributor.authorSayin, Niyazi Cenk
dc.contributor.authorGurkan, H.
dc.contributor.authorCiftdemir, N. A.
dc.contributor.authorAtli, E.
dc.contributor.authorInan, C.
dc.contributor.authorErzincan, S.
dc.contributor.authorSutcu, H.
dc.contributor.authorVatansever, U.
dc.contributor.authorVarol, Fusun
dc.date.accessioned2019-06-24T11:15:56Z
dc.date.available2019-06-24T11:15:56Z
dc.date.issued2018
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Anabilim Dalıen_US
dc.descriptionCilingir, I. Uzun (Trakya Author) Sayin, Niyazi Cenk (Trakya Author) Gurkan, H.(Trakya Author) Ciftdemir, N. A. (Trakya Author) Atli, E. (Trakya Author) Inan, C. (Trakya Author) Erzincan, S. (Trakya Author) Sutcu, H. (Trakya Author) Vatansever, U. (Trakya Author) Varol, Fusun (Trakya Author)en_US
dc.description.abstractMacro Domain Containing 2 (MACRO D2) gene is a gene from macro family which is highly expressed in the ventriculer zone of the brain during embryonic development. Association between Autism spectrum disorders and MACRO D2 gene polymorphisms has been reported before [1] . Deletion in MACRO D2 gene has also been associated with Kabuki Syndrome which is a well described congential anomaly syndrome [2] .en_US
dc.identifier.citationUzun, Ç. I., Sayin, N. C., Gurkan, H., Çiftdemir, N. A., Atlı, E., İnan, C., ... & Varol, F. (2018). Deletion of macro domain containing 2 (MACRO D2) associated with transient hydrops fetalis. Taiwanese journal of obstetrics & gynecology, 57(6), 897.en_US
dc.identifier.doi10.1016/j.tjog.2018.10.023en_US
dc.identifier.endpage898en_US
dc.identifier.issue6en_US
dc.identifier.pmid30545550en_US
dc.identifier.scopus2-s2.0-85055887810en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage897en_US
dc.identifier.urihttps://doi.org/10.1016/j.tjog.2018.10.023
dc.identifier.urihttps://hdl.handle.net/20.500.14551/4183
dc.identifier.volume57en_US
dc.identifier.wosWOS:000455098000025en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherElsevier Taiwanen_US
dc.relation.ispartofJournal Citation Reportsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.snmz20240608_ID_Qen_US
dc.subjectHydrops Fetalisen_US
dc.subjectKabuki Syndromeen_US
dc.subjectMacro D2 geneen_US
dc.subjectEtiologyen_US
dc.subjectGeneen_US
dc.titleDeletion of macro domain containing 2(MACRO D2) associated with transient hydrops fetalisen_US
dc.typeArticleen_US

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