Turner Syndrome and Its Variants by Semra Gürsoy, Derya Erçal

Get full text

Expanding spectrum of SCN1A-related phenotype with novel mutations by Semra Hız-Kurul, Semra Gürsoy, Müge Ayanoğlu, Uluç Yiş, Derya Erçal

Get full text

Correction: Demir et al. Retrospective analysis of pregnancy terminations and indications in a tertiary center. Clinical and Experimental Obstetrics & Gynecology. 2021; 48: 85–90 by Sureyya Saridas Demir, Erkan Cağliyan, Sabahattin Altunyurt, Tufan Çankaya, Elçin Bora, Derya Erçal

Get full text

Congenital cardiac defects with 22q11 deletion by Ozlem Giray, Ayfer Ulgenalp, Elçin Bora, Gül Sağin Saylam, Nurettin Unal, Timur Meşe, Suphi Hüdaoğlu, Derya Erçal

Get full text

Evaluation of Associated Structural and Chromosomal Abnormalities in Patients with Fetal Cerebral Ventriculomegaly Detected in Ultrasonographic Imaging by Erkan Cagliyan, Samican Ozmen, Sureyya Saridas Demir, Ceren Aydin, Egehan Bilen, Handan Guleryuz, Elif Yasar, Derya Ercal, Elcin Bora, Tufan Cankaya

Get full text

Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy by Ayfer Ulgenalp, Ferda Ozkinay, Eray Dirik, Sarenur Tütüncüoğlu, Gülşen Dizdarer, Nedret Uran, Hatice Karasoy, Gül Sağin-Saylam, Semra Kurul, Tülin Hizli, Elçin Bora, Ozlem Giray, Derya Erçal

Get full text