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FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis
Poster Presentations
FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis
J Clin Res Pediatr Endocrinol 2017;9(1):21-21
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- 1Ege University Faculty Of Medicine, Department Of Medical Genetics, Izmir, Turkey
- 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
Corresponding Author: Ege University Faculty Of Medicine, Department Of Medical Genetics, Izmir, Turkey
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