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

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dc.contributor.authorGÜRAN, TÜLAY
dc.contributor.authorDEMİRCİOĞLU, SERAP
dc.contributor.authorBEREKET, ABDULLAH
dc.contributor.authorsAbali Z. Y. , Ates E. A. , GÜRAN T., BEREKET A., DEMİRCİOĞLU S.
dc.date.accessioned2022-10-10T16:54:36Z
dc.date.available2022-10-10T16:54:36Z
dc.date.issued2022-09-01
dc.identifier.citationAbali 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
dc.identifier.endpage230
dc.identifier.issn1663-2818
dc.identifier.issueSUPPL 2
dc.identifier.startpage230
dc.identifier.urihttps://hdl.handle.net/11424/282238
dc.identifier.volume95
dc.language.isoeng
dc.relation.ispartofHORMONE RESEARCH IN PAEDIATRICS
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectMedicine
dc.subjectInternal Medicine Sciences
dc.subjectChild Health and Diseases
dc.subjectInternal Diseases
dc.subjectEndocrinology and Metabolic Diseases
dc.subjectHealth Sciences
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectPEDİATRİ
dc.subjectENDOCRINOLOGY & METABOLISM
dc.subjectCLINICAL MEDICINE
dc.subjectClinical Medicine (MED)
dc.subjectPEDIATRICS
dc.subjectPediatri
dc.subjectEndokrin ve Otonom Sistemler
dc.subjectPediatri, Perinatoloji ve Çocuk Sağlığı
dc.subjectEndokrinoloji, Diyabet ve Metabolizma
dc.subjectEndokrinoloji
dc.subjectYaşam Bilimleri
dc.subjectPediatrics
dc.subjectEndocrine and Autonomic Systems
dc.subjectPediatrics, Perinatology and Child Health
dc.subjectEndocrinology, Diabetes and Metabolism
dc.subjectEndocrinology
dc.subjectLife Sciences
dc.titleA rare cause of monogenic obesity: Schaaf-Yang syndrome due to a novel MAGEL2 gene variant
dc.typearticle
dspace.entity.typePublication
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