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Sotos syndrome is characterized by overgrowth, macrocephaly, distinctive facial features, and learning disabilities and is associated with alterations in the nuclear receptor binding SET domain protein 1 (NSD1) gene. Due to the advanced bone age, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9651::7ffcb3b3b12ebc47e66941e2259aa0da
http://hdl.handle.net/20.500.12645/28552
http://hdl.handle.net/20.500.12645/28552
Autor:
Diri, H.1 halitdiri@yahoo.com, Sener, E. F.2, Bayram, F.1, Dundar, M.3, Simsek, Y.1, Baspinar, O.4, Zararsiz, G.5
Publikováno v:
Acta Endocrinologica (1841-0987). Oct-Dec2016, Vol. 12 Issue 4, p413-417. 5p.
Akademický článek
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Autor:
Bulbul E; Kayseri Training and Research Hospital, Department of Emergency Medicine, Kayseri, Turkey., Sener EF; Erciyes University, Faculty of Medicine, Department of Medical Biology, Kayseri, Turkey., Gunay NE; Kayseri Training and Research Hospital, Department of Clinical Biochemistry, Kayseri, Turkey., Taslidere B; Malatya State Hospital, Department of Emergency Medicine, Malatya, Turkey., Taslidere E; Bezmialem Vakif University, Faculty of Medicine, Department of Histology and Embryology, İstanbul, Turkey., Koyuncu S; Gaziosmanpasa University, Faculty of Medicine, Department of Emergency Medicine, Tokat, Turkey., Gunay N; Erciyes University, Faculty of Medicine, Department of Emergency Medicine, Kayseri, Turkey. Electronic address: ngunay@erciyes.edu.tr.
Publikováno v:
The American journal of emergency medicine [Am J Emerg Med] 2019 May; Vol. 37 (5), pp. 1008. Date of Electronic Publication: 2018 Oct 25.