TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy by Feryal Cabuk, Halil G Karabulut, Timur Tuncali, Selmin Karademir, Mithat Bozdayi, Ajlan Tükün

Get full text

Nuchal Translucency Measurement Did Not Significantly Predict Trisomy Cases in Tertiary Referral Center by Tülay Tos, Enis Özkaya, Vakkas Korkmaz, Yeşim Özkaya, Ajlan Tukun, Oya Gökmen, Tuncay Küçüközkan

Get full text

Concomitant Alpha- and Gamma-Sarcoglycan Deficiencies in a Turkish Boy with a Novel Deletion in the Alpha-Sarcoglycan Gene by Gulden Diniz, Hulya Tosun Yildirim, Sarenur Gokben, Gul Serdaroglu, Filiz Hazan, Kanay Yararbas, Ajlan Tukun

Get full text

ACE gene deletion/deletion polymorphism may be a protective factor for respiratory distress in preterm infants by Ercan Sivasli, Murat Yurdakök, Elif Babaoğlu, Halil Karabulut, Sule Yiğit, Melih Babaoğlu, Gülsevin Tekinalp, Ajlan Tükün

Get full text

Association Between N363S and BclI Polymorphisms of the Glucocorticoid Receptor Gene (NR3C1) and Glucocorticoid Side Effects During Childhood Acute Lymphoblastic Leukemia Treatment by Meriç Kaymak Cihan, Halil Gürhan Karabulut, Nüket Yürür Kutlay, Hatice Ilgın Ruhi, Ajlan Tükün, Lale Olcay

Get full text

Chronic eosinophilic leukemia with monosomy 8 in a five-year-old girl: a rare case by Meriç Kaymak-Cihan, Macit Arıyürek, Nural Kiper, Ayşenur Paç, Nazire Terzi, Serpil Dizbay-Sak, Işınsu Kuzu, Bilgin Arıbaş, Barış Kuşkonmaz, Ajlan Tükün, Lale Olcay

Get full text