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Ventricular septal defect closure in a patient with VACTERL syndrome - Anticipating sequelae in a rare genetic disorder

dc.contributor.authorHatemi, Ali Can
dc.contributor.authorGursoy, Mete
dc.contributor.authorÇelebi, Mustafa Serdar
dc.contributor.authorKansiz, Erhan
dc.contributor.authorCetin, Gurkan
dc.contributor.authorTongut, Aybala
dc.contributor.authorCeviker, Kadir
dc.date.accessioned2021-03-03T12:54:06Z
dc.date.available2021-03-03T12:54:06Z
dc.date.issued2008
dc.identifier.citationHatemi A. C. , Gursoy M., Ceviker K., Tongut A., Cetin G., Çelebi M. S. , Kansiz E., "Ventricular septal defect closure in a patient with VACTERL syndrome - Anticipating sequelae in a rare genetic disorder", TEXAS HEART INSTITUTE JOURNAL, cilt.35, sa.2, ss.203-205, 2008
dc.identifier.issn1526-6702
dc.identifier.otherav_30b37566-4e80-4a9e-ad76-86ed2d6d1471
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/37213
dc.description.abstractNoncardiac components of genetic disorders can complicate the operative and postoperative courses of pediatric cardiac surgery patients. Prolonged hospital stay increased treatment cost, morbidity, and death are more likely in this subgroup of patients.
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectKardiyoloji
dc.titleVentricular septal defect closure in a patient with VACTERL syndrome - Anticipating sequelae in a rare genetic disorder
dc.typeMakale
dc.relation.journalTEXAS HEART INSTITUTE JOURNAL
dc.contributor.departmentİstanbul Teknik Üniversitesi , Bilişim Enstitüsü ,
dc.identifier.volume35
dc.identifier.issue2
dc.identifier.startpage203
dc.identifier.endpage205
dc.contributor.firstauthorID185783


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