Turner Syndrome and Its Variants by Semra Gürsoy, Derya Erçal

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The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome by Semra Gürsoy, Yaşar Bekir Kutbay, Taha Reşid Özdemir, Filiz Hazan

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Neonatal bacterial meningitis in Turkey: epidemiology, risk factors, and prognosis by Sultan Kavuncuoğlu, Semra Gürsoy, Özden Türel, Esin Yildiz Aldemir, Emine Hoşaf

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

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A Rare Case of Cystic Hygroma and Familial Nystagmus in a Newborn with SHOC2 Gene Mutation by Suzan Süncak, Filiz Hazan, Coşkun Armağan, Ceren Yılmaz Uzman, Semra Gürsoy, Özlem Giray Bozkaya

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A newborn with monosomy X in association with corpus callosum agenesis by Duygu Onur Cura, Burcin Iscan, Semra Gursoy, Handan Guleryuz, Tufan Cankaya, Tulay Ozturk, Ozlem Giray Bozkaya

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The effects of epigenetic regulation on phenotypic expressivity in Turkish patients with familial Mediterranean fever by Eser Dogan, Semra Gursoy, Giray Bozkaya, Secil Arslansoyu Camlar, Ozge Aksel Kilicarslan, Alper Soylu, Ayfer Ulgenalp, Salih Kavukcu, Ozlem Giray Bozkaya

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A novel compound heterozygous variant in CYP19A1 resulting in aromatase deficiency with normal ovarian tissue by Sezer Acar, Ece Böber, Mustafa Olguner, Erdener Özer, Ayhan Abacı, Bayram Özhan, Semra Gürsoy, Tufan Çankaya, Hüseyin Onay, Ahu Paketçi, İbrahim Mert Erbaş, Korcan Demir

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