Long-Term Follow-Up Outcomes of 19 Patients with Osteogenesis Imperfecta Type XI and Bruck Syndrome Type I Caused by FKBP10 Variants von Yüksel Ülker, Aylin, Uludağ Alkaya, Dilek, Elkanova, Leyla, Şeker, Ali, Akpınar, Evren, Akarsu, Nurten Ayşe, Uyguner, Zehra Oya, Tüysüz, Beyhan

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An investigation of the etiology and follow‐up findings in 35 children with overgrowth syndromes, including biallelic SUZ12 variant von Yüksel Ülker, Aylin, Uludağ Alkaya, Dilek, Çağlayan, Ahmet Okay, Usluer, Esra, Aykut, Ayça, Aslanger, Ayça, Vural, Mehmet, Tüysüz, Beyhan

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Congenital Heart Defects and Outcome in a Large Cohort of Down Syndrome: A Single-Center Experience from Turkey von Uludağ Alkaya, Dilek, Öztürk, Birol, Yüksel Ülker, Aylin, Bozlak, Serdar, Öztürk, Esra, Dedeoğlu, Reyhan, Eroğlu, Ayşe Güler, Öztunç, Funda, Tüysüz, Beyhan

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A Large Turkish Cohort of Williams Syndrome: The Evaluation of Facial, Cardiovascular, and Neuropsychiatric Features von Bozlak, Serdar, Uludağ Alkaya, Dilek, Kasap, Büşra, Yüksel Ülker, Aylin, Yıldız, Ceren Ayça, Altındağ, Veysel, Ülkersoy, İpek, Çifçi Sunamak, Evrim, Dedeoğlu, Reyhan, Tüysüz, Beyhan

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The Clinical and Molecular Spectrum of Trichorhinophalangeal Syndrome Types I and II in a Turkish Cohort Involving 22 Patients von Güneş, Nilay, Usluer, Esra, Yüksel Ülker, Aylin, Uludağ Alkaya, Dilek, Çifçi Sunamak, Evrim, Celep Eyüpoğlu, Figen, Uyguner, Zehra Oya, Tüysüz, Beyhan

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