机译:婴儿在11p15号染色体上的父母单亲二体性的先天性高胰岛素血症:提示贝克威-维德曼综合征的临床特征很少
Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan;
Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan;
Division of Molecular Genetics and Epigenetics, Department of Biomolecular Sciences, Saga University, Saga, Japan;
Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan;
Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan;
Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan;
Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan;
Division of Molecular Genetics and Epigenetics, Department of Biomolecular Sciences, Saga University, Saga, Japan;
Department of Pediatrics, Kizawa Memorial Hospital, Gifu, Japan;
Department of Radiology, Kizawa Memorial Hospital, Gifu, Japan;
Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan;
Division of Molecular Genetics and Epigenetics, Department of Biomolecular Sciences, Saga University, Saga, Japan;
beckwith-wiedemann syndrome; congenital hyperinsulinism; ~(18)f-fiuoro-L-DOPA positron emission tomography; uniparental disomy 11 p15;
机译:婴儿在11p15号染色体上的父母单亲二联症的先天性高胰岛素血症:很少有临床特征提示贝克威-维德曼综合征
机译:婴儿科斯特洛综合征的胰腺结节中的家长单亲二体性11p15.5:柯斯特洛和贝克维斯-维德曼综合征的新生儿高胰岛素低血糖的共同机制以及科斯特洛综合征驱动克隆扩展的体细胞杂合性丧失
机译:两名患有镶嵌单亲二体性11p的Beckwith-Wiedemann综合征的患者持续存在先天性高胰岛素血症
机译:磁化转移率(MTR)提示多发性硬化的临床孤立综合征(CIS)患者脑组织病理学改变的预后价值
机译:限制碳水化合物摄入和美国心脏协会饮食对阿联酋年轻成年人代谢综合征的临床特征,炎症反应和脂蛋白代谢的影响
机译:患有Beckwith-Wiedemann综合征的患者的肝母细胞瘤的基因组特征染色体11p15上具有单亲二体性APC和PALB2的种系突变
机译:先天性高胰岛素在患有父亲的染色体上的婴儿11p15:临床特征暗示贝克韦氏症综合征