Genetic etiology in patients diagnosed with congenital hypothyroidism with new-generation sequencing: A single-center experience von Aytaç Kaplan, Emel Hatun, Mermer, Serdar

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Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience von Esen, İhsan, Bayramoğlu, Elvan, Yıldız, Melek, Aydın, Murat, Karakılıç Özturhan, Esin, Aycan, Zehra, Bolu, Semih, Önal, Hasan, Kör, Yılmaz, Ökdemir, Deniz, Ünal, Edip, Önder, Aşan, Evliyaoğlu, Olcay, Çayır, Atilla, Taştan, Mehmet, Yüksel, Ayşegül, Kılınç, Aylin, Büyükinan, Muammer, Özcabı, Bahar, Akın, Onur, Binay, Çiğdem, Kılınç, Suna, Yıldırım, Ruken, Aytaç, Emel Hatun, Sağsak, Elif

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Pediatric hypoparathyroidism: etiological and clinical evaluation in a tertiary center von Kocabey Sütçü, Zümrüt, Aytaç Kaplan, Emel Hatun, Önal, Hasan

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Genotype-biochemical phenotype analysis in newborns with biotinidase deficiency in Southeastern Anatolia von Karaoglan, Murat, Nacarkahya, Gulper, Aytac, Emel Hatun, Keskin, Mehmet

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Case Report of Leri-Weill Dyscontrosteosis Caused By SHOX Gene Deletion von Emel Hatun Aytaç Kaplan, Keskin, Mehmet, Melik, Melda

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Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia von Karaoglan, Murat, Nacarkahya, Gulper, Aytac, Emel Hatun, Keskin, Mehmet

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Management of thyrotoxicosis in children and adolescence: a Turkish multi-center experience von Esen, Ihsan, Bayramoğlu, Elvan, Yıldız, Melek, Aydın, Murat, Karakılıç Özturhan, Esin, Aycan, Zehra, Bolu, Semih, Önal, Hasan, Kör, Yılmaz, Ökdemir, Deniz, Ünal, Edip, Önder, Aşan, Evliyaoğlu, Olcay, Çayır, Atilla, Taştan, Mehmet, Yüksel, Ayşegül, Kılınç, Aylin, Büyükinan, Muammer, Özcabı, Bahar, Akın, Onur, Binay, Çiğdem, Kılınç, Suna, Yıldırım, Ruken, Aytaç, Emel Hatun, Sağsak, Elif

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Case Report of Leri-Weill Dyscontrosteosis Caused By SHOX Gene Deletion von Kaplan, Emel Hatun Aytac, Keskin, Mehmet, Melik, Melda

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