Search Results - Oya Uyguner

Association of AXIN2 gene polymorphisms with nonsyndromic oligodontia in Turkish families by Nuriye Dinckan, Zehra Oya Uyguner, Hulya Kayserili, Ariadne Letra

Connect to this object online.

GG Polymorphism of Platelet ITGA2B Gene Increases the Magnitude of Interleukin-6 Release after Cardiopulmonary Bypass by Koray Ak, Samet Ergun, Hilal Altınoz, Z Oya Uyguner, Sermin Tetik

Connect to this object online.

Nance-Horan Syndrome: characterization of dental, clinical and molecular features in three new families by Yeliz Guven, Hilal Piril Saracoglu, Sermin Dicle Aksakal, Tugba Kalayci, Umut Altunoglu, Zehra Oya Uyguner, Serpil Eraslan, Esra Borklu, Hulya Kayserili

Connect to this object online.

"Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports" by Fahrettin Uysal, Burcu Turkgenc, Guven Toksoy, Ozlem M. Bostan, Elif Evke, Oya Uyguner, Cengiz Yakicier, Hulya Kayserili, Ergun Cil, Sehime G. Temel

Connect to this object online.

Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD by Neşe Akcan, Oya Uyguner, Firdevs Baş, Umut Altunoğlu, Güven Toksoy, Birsen Karaman, Şahin Avcı, Zehra Yavaş Abalı, Şükran Poyrazoğlu, Agharza Aghayev, Volkan Karaman, Rüveyde Bundak, Seher Başaran, Feyza Darendeliler

Connect to this object online.

PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency by Aslı Derya Kardelen, Adam Najaflı, Firdevs Baş, Birsen Karaman, Güven Toksoy, Şükran Poyrazoğlu, Şahin Avcı, Umut Altunoğlu, Zehra Yavaş Abalı, Ayşe Pınar Öztürk, Esin Karakılıç Özturan, Seher Başaran, Feyza Darendeliler, Z. Oya Uyguner

Connect to this object online.