An unusual case of monosomy 18p: minor malformations with speech delay por Elçin Bora, Ozlem Giray, Ayfer Ulgenalp, Hasan Ozkan, Derya Erçal

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A Rare Karyotype of Turner Syndrome: 45.X/47.XXX por Ayça Altıncık, Gönül Çatlı, Korcan Demir, Ayhan Abacı, Elçin Bora, Derya Erçal, Ece Böber

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Lack of Association of Childhood Partial Epilepsy with Brain Derived Neurotrophic Factor Gene por Aycan Unalp, Elcin Bora, Tufan Cankaya, Ozlem Giray Bozkaya, Derya Ercal, Aysel Ozturk, Ayfer Ulgenalp

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

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Clinical and Molecular Analysis in Patients with Peutz-Jeghers Syndrome por Pınar Günay Aslan, Ahmet Oktay Çağlayan, Elçin Bora, Altuğ Koç, Hilal Yücel, Ayfer Ülgenalp, Yeşil Öztürk, Gül Şeker, Mesut Akarsu

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

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Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy por 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

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