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Turkish Journal of Medical Sciences

DOI

-

Abstract

ILIÇ^1, Yıldırım BAYKARA^1, C. Nur SEMERCİ^2, Hacer ERGİN^1, N. Lale ŞATIROĞLU TUFAN^2 ^1 Department of Pediatrics, Faculty of Medicine, Pamukkale University, Denizli - Turkey ^2 Department of Medical Biology, Genetics Unit, Faculty of Medicine, Pamukkale University, Denizli - Turkey

Keywords

Apert syndrome, FGFR2 mutation

First Page

405

Last Page

408

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