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Apert Sendromu ve Atriyal Septal Defekt Birlikteliği

dc.contributor.authorDervişoğlu Çavdaroğlu, Pınar
dc.contributor.authorKösecik, Mustafa
dc.contributor.authorKumbasar, Serkan
dc.contributor.authorSalman, Süleyman
dc.contributor.authorAytek sık, Bulat
dc.contributor.authorErdem, Baki
dc.contributor.authorTekin, Bülent
dc.date.accessioned2021-12-21T08:31:55Z
dc.date.available2021-12-21T08:31:55Z
dc.date.issued2016
dc.identifier.issn2146-6505
dc.identifier.issn2147-1894
dc.identifier.urihttps://app.trdizin.gov.tr/makale/TWpBMk5qZ3hNUT09/apert-sendromu-ve-atriyal-septal-defekt-birlikteligi
dc.identifier.urihttp://dspace.yeniyuzyil.edu.tr:8080/xmlui/handle/20.500.12629/896
dc.description.abstractApert sendromu kraniyosinostoz, yüzün orta kısmında hipoplazi, el ve ayaklarda simetrik sindaktili ve değişen derecelerde mental retardasyon ve konjenital kalp defektleri ile karakterize nadir bir bozukluktur. Kalıtım şekli otozomal dominant olmakla birli
dc.description.abstractApert syndrome, craniosynostosis, mid-face hypoplasia, symmetric syndactyly of the hands and feet, and varying degrees of mental retardation, and is characterized by congenital heart defects. Although the mode of inheritance is autosomal dominant, it crea
dc.language.isoTurkish
dc.titleApert Sendromu ve Atriyal Septal Defekt Birlikteliği
dc.title.alternativeAssociation between Apert Syndrome and Atrial Septal Defect
dc.relation.journalJAREM
dc.identifier.issue3
dc.identifier.startpage200
dc.identifier.endpage202
dc.identifier.volume6
dc.relation.issue3
dc.relation.volume6


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