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A rare cause of monogenic obesity: Schaaf-Yang syndrome due to a novel MAGEL2 gene variant

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2022-09-01

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Tıp, Dahili Tıp Bilimleri, Çocuk Sağlığı ve Hastalıkları, İç Hastalıkları, Endokrinoloji ve Metabolizma Hastalıkları, Sağlık Bilimleri, Medicine, Internal Medicine Sciences, Child Health and Diseases, Internal Diseases, Endocrinology and Metabolic Diseases, Health Sciences, ENDOKRİNOLOJİ VE METABOLİZMA, Klinik Tıp, Klinik Tıp (MED), PEDİATRİ, ENDOCRINOLOGY & METABOLISM, CLINICAL MEDICINE, Clinical Medicine (MED), PEDIATRICS, Pediatri, Endokrin ve Otonom Sistemler, Pediatri, Perinatoloji ve Çocuk Sağlığı, Endokrinoloji, Diyabet ve Metabolizma, Endokrinoloji, Yaşam Bilimleri, Pediatrics, Endocrine and Autonomic Systems, Pediatrics, Perinatology and Child Health, Endocrinology, Diabetes and Metabolism, Endocrinology, Life Sciences

Citation

Abali Z. Y. , Ates E. A. , GÜRAN T., BEREKET A., DEMİRCİOĞLU S., "A rare cause of monogenic obesity: Schaaf-Yang syndrome due to a novel MAGEL2 gene variant", HORMONE RESEARCH IN PAEDIATRICS, cilt.95, sa.SUPPL 2, ss.230, 2022

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https://hdl.handle.net/11424/282238

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