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Correction to: Global gene expression profiling in congenital diaphragmatic hernia (CDH) patients (Functional & Integrative Genomics, (2022), 22, 3, (359-369), 10.1007/s10142-022-00837-9)

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dc.contributor.author Gürünlüoğlu, K.
dc.contributor.author Dündar, M.
dc.contributor.author Unver, T.
dc.contributor.author Akpınar, N.
dc.contributor.author Gokce, I.K.
dc.contributor.author Gürünlüoğlu, S.
dc.contributor.author Demircan, M.
dc.contributor.author Koc, A.
dc.date.accessioned 2022-10-06T12:54:14Z
dc.date.available 2022-10-06T12:54:14Z
dc.date.issued 2022
dc.identifier.issn 1438793X (ISSN)
dc.identifier.uri http://hdl.handle.net/11616/72059
dc.description.abstract In the Introduction part, 4th sentence, "It is thought to be caused by a developmental defect of the pleuroperitoneal membrane, one of the four parts of the diaphragm (Ameis et al. 2017)" should be replaced with: "Its cause has not been fully known but genetic defects are thought to play roles in the etiology due to its emergence in the early period (embryologic); lung and heart anomalies frequently accompanied by this disease (Ameis et al. 2017)". The original article has been corrected. © 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
dc.source Functional and Integrative Genomics
dc.title Correction to: Global gene expression profiling in congenital diaphragmatic hernia (CDH) patients (Functional & Integrative Genomics, (2022), 22, 3, (359-369), 10.1007/s10142-022-00837-9)


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