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pro vyhledávání: '"Baranoski, Jacob E."'
Autor:
Caglayan, Ahmet Okay, Baranoski, Jacob E., Aktar, Fesih, Han, Wengi, Tuysuz, Beyhan, Guzel, Asian, Guclu, Bulent, Kaymakcalan, Hande, Aktekin, Berrin, Akgumus, Gozde Tugce, Murray, Phillip B., Erson-Omay, Emine Z., Caglar, Caner, Bakircioglu, Mehmet, Sakalar, Yildirim Bayezit, Guzel, Ebru, Demir, Nihat, Tuncer, Oguz, Senturk, Senem, Ekici, Saris
BACKGROUND: Knobloch syndrome is a rare, autosomal recessive, developmental disorder characterized by stereotyped ocular abnormalities with or without occipital skull deformities (encephalocele, bone defects, and cutis aplasia). Although there is cle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=r39c86a4b39b::1ba65f35c0f0e3417be9f3c315c2294f
https://aperta.ulakbim.gov.tr/record/64339
https://aperta.ulakbim.gov.tr/record/64339