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

GÜRAN, TÜLAYDEMİRCİOĞLU, SERAPBEREKET, ABDULLAH2022-10-102022-10-102022-09-01Abali 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, 20221663-2818https://hdl.handle.net/11424/282238enginfo:eu-repo/semantics/openAccessTıpDahili Tıp BilimleriÇocuk Sağlığı ve Hastalıklarıİç HastalıklarıEndokrinoloji ve Metabolizma HastalıklarıSağlık BilimleriMedicineInternal Medicine SciencesChild Health and DiseasesInternal DiseasesEndocrinology and Metabolic DiseasesHealth SciencesENDOKRİNOLOJİ VE METABOLİZMAKlinik TıpKlinik Tıp (MED)PEDİATRİENDOCRINOLOGY & METABOLISMCLINICAL MEDICINEClinical Medicine (MED)PEDIATRICSPediatriEndokrin ve Otonom SistemlerPediatri, Perinatoloji ve Çocuk SağlığıEndokrinoloji, Diyabet ve MetabolizmaEndokrinolojiYaşam BilimleriPediatricsEndocrine and Autonomic SystemsPediatrics, Perinatology and Child HealthEndocrinology, Diabetes and MetabolismEndocrinologyLife SciencesA rare cause of monogenic obesity: Schaaf-Yang syndrome due to a novel MAGEL2 gene variantarticle95SUPPL 2230230