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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 discover
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43dc6207e2533a5824de54d287aeb059
https://aperta.ulakbim.gov.tr/record/233554
https://aperta.ulakbim.gov.tr/record/233554