ISSN: 1308-5727 | E-ISSN: 1308-5735
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Abstracting & Indexing
Turkish Society for Pediatric Endocrinology and Diabetes
J Clin Res Pediatr Endocrinol. 2017; 9(1): 21-21
2Bezmialem Vakif University Faculty Of Medicine, Department Of Medical Genetics, Istanbul, Turkey
3Dr. Behçet Uz Children’S Hospital, Clinic Of Medical Genetics, Izmir, Turkey
4Kayseri Training And Research Hospital, Clinic Of Medical Genetics, Kayseri, Turkey
5Istanbul University Cerrahpasa Faculty Of Medicine, Department Of Pediatric Genetics, Istanbul, Turkey
6Erciyes University Faculty Of Medicine, Department Of Medical Genetics, Kayseri, Turkey
FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis
Emine Ipek Ceylan1, Asli Ece Solmaz1, Hüseyin Onay1, Ayça Aykut1, Asude Durmaz1, Gözde Yesil2, Filiz Hazan3, Aslihan Kiraz4, Beyhan Tüysüz5, Meltem Cerrah Günes61Ege University Faculty Of Medicine, Department Of Medical Genetics, Izmir, Turkey2Bezmialem Vakif University Faculty Of Medicine, Department Of Medical Genetics, Istanbul, Turkey
3Dr. Behçet Uz Children’S Hospital, Clinic Of Medical Genetics, Izmir, Turkey
4Kayseri Training And Research Hospital, Clinic Of Medical Genetics, Kayseri, Turkey
5Istanbul University Cerrahpasa Faculty Of Medicine, Department Of Pediatric Genetics, Istanbul, Turkey
6Erciyes University Faculty Of Medicine, Department Of Medical Genetics, Kayseri, Turkey
Emine Ipek Ceylan, Asli Ece Solmaz, Hüseyin Onay, Ayça Aykut, Asude Durmaz, Gözde Yesil, Filiz Hazan, Aslihan Kiraz, Beyhan Tüysüz, Meltem Cerrah Günes. FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis. J Clin Res Pediatr Endocrinol. 2017; 9(1): 21-21
Manuscript Language: English
Manuscript Language: English
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