机译:评价CHD7变异性CHD7变体的先天性腺增生性腺性腺低因素患者的电荷综合征。
Endocrinology Diabetology &
Metabolism Service Lausanne University Hospital Lausanne Switzerland;
Endocrinology Diabetology &
Metabolism Service Lausanne University Hospital Lausanne Switzerland;
Institute for Research in Immunology and Cancer University of Montreal Montreal Canada;
Institute for Genetic Medicine University of Newcastle-on-Tyne Newcastle-on Tyne UK;
Endocrinology-Diabetology Unit Department of Paediatrics Lausanne University Hospital Lausanne;
Clinic of Gynecological Endocrinology and Reproductive Medicine University Hospital University of;
Division of Pediatric Endocrinology and Diabetology Department of Pediatrics and Department of;
Division of Endocrinology Diabetes and Clinical Nutrition Inselspital Bern University Hospital;
Department of Human Genetics Inselspital Bern University Hospital and University of Bern Bern;
Department of Endocrinology St John's Hospital Budapest Hungary;
Department of Endocrinology Hospital Clínic Universitat de Barcelona Barcelona Spain;
Clinic of Endocrinology Diabetes and Diseases of Metabolism University Clinical Center Belgrade;
Department of Radiology Lausanne University Hospital Lausanne Switzerland;
Endocrinology Diabetology &
Metabolism Service Lausanne University Hospital Lausanne Switzerland;
Endocrinology Diabetology &
Metabolism Service Lausanne University Hospital Lausanne Switzerland;
Endocrinology Diabetology &
Metabolism Service Lausanne University Hospital Lausanne Switzerland;
Endocrinology Diabetology &
Metabolism Service Lausanne University Hospital Lausanne Switzerland;
Department of Endocrinology Hospital S Jo?o Porto Portugal;
Endocrinology Diabetology &
Metabolism Service Lausanne University Hospital Lausanne Switzerland;
Endocrinology Diabetology &
Metabolism Service Lausanne University Hospital Lausanne Switzerland;
Endocrinology Diabetology &
Metabolism Service Lausanne University Hospital Lausanne Switzerland;
CHARGE syndrome; Kallmann syndrome; chromodomain helicase DNA binding protein 7; congenital hypogonadotropic hypogonadism;
机译:评价CHD7变异性CHD7变体的先天性腺增生性腺性腺低因素患者的电荷综合征。
机译:突尼斯人患有两个罕见综合征:三重综合征和先天性性腺功能减退性腺功能减退症
机译:先天性促性腺激素性性腺功能减退/卡尔曼综合征的男性中的胰岛素样肽3(INSL3)和激素治疗的不同方式的影响:281例患者的单中心研究
机译:zCare:设计一种移动应用程序以支持先天性寨卡综合征患者的护理人员
机译:遗传学评估对疑似埃勒斯-丹洛斯综合症或其他可能的结缔组织病患者的价值
机译:GnRH缺乏先天性腺增黄缺发性低因素的患者:ANOS1RNF216WDR11FGFR1CHD7和POLR3A基因的新型遗传发现以及文献审查
机译:先天性腺增生缺血性腺性腺低因素患者评估含CHD7变异的电荷综合征