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Vargel, Ibrahim; Canter, Halil Ibrahim; Kucukguven, Arda; Aydin, Asim; Ozgur, Figen
{ "DOI": "10.1177/10556656211019621", "abstract": "Aim: The term frontonasal dysplasia (FND) represents a spectrum of anomalies and its genetics have not been well defined. Recently, the critical role of the aristaless-like homeobox (ALX) gene family on the craniofacial development has been discovered. In the present study, we aimed to propose a systematic surgical treatment plan for the ALX-related FNDs according to the genotypic classification as well as demonstrating their clinical characteristics to help surgeons diagnose the underlying pathology accurately.", "author": [ { "family": "Vargel", "given": " Ibrahim" }, { "family": "Canter", "given": " Halil Ibrahim" }, { "family": "Kucukguven", "given": " Arda" }, { "family": "Aydin", "given": " Asim" }, { "family": "Ozgur", "given": " Figen" } ], "container_title": "CLEFT PALATE-CRANIOFACIAL JOURNAL", "id": "233554", "issue": "5", "issued": { "date-parts": [ [ 2022, 1, 1 ] ] }, "page": "637-643", "title": "ALX-Related Frontonasal Dysplasias: Clinical Characteristics and Surgical Management", "type": "article-journal", "volume": "59" }
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