Association between Apert Syndrome and Atrial Septal Defect

dc.contributor.author	Dervisoglu, Pinar
dc.contributor.author	Kosecik, Mustafa
dc.contributor.author	Kumbasar, Serkan
dc.contributor.author	Salman, Suleyman
dc.contributor.author	Sik, Bulat Aytek
dc.contributor.author	Erdem, Baki
dc.contributor.author	Tekin, Bulent
dc.date.accessioned	2021-12-21T08:47:48Z
dc.date.available	2021-12-21T08:47:48Z
dc.date.issued	2016
dc.identifier.issn	2146-6505
dc.identifier.issn	2147-1894
dc.identifier.uri	https://doi.org/10.5152/jarem.2016.896
dc.identifier.uri	http://dspace.yeniyuzyil.edu.tr:8080/xmlui/handle/20.500.12629/2305
dc.description.abstract	Apert 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.iso	Turkish
dc.publisher	Aves
dc.title	Association between Apert Syndrome and Atrial Septal Defect
dc.type	Article
dc.relation.journal	Journal Of Academıc Research In Medıcıne-Jarem
dc.identifier.issue	3
dc.identifier.startpage	200
dc.identifier.endpage	202
dc.identifier.volume	6
dc.identifier.doi	10.5152/jarem.2016.896
dc.relation.issue	3
dc.relation.volume	6

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