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机译:中国胶原蛋白VI相关肌病患者群组遗传和临床调查结果
Department of PediatricsPeking University First HospitalBeijing China;
Department of PediatricsPeking University First HospitalBeijing China;
Department of PediatricsPeking University First HospitalBeijing China;
Department of PediatricsPeking University First HospitalBeijing China;
Department of PediatricsPeking University First HospitalBeijing China;
Department of PediatricsPeking University First HospitalBeijing China;
Department of NeurologyPeking University First HospitalBeijing China;
Neuromuscular and Neurogenetic Disorders of Childhood SectionNational Institute of Neurological;
Human Genetics Resources Core FacilitySchool of Life Sciences Peking UniversityBeijing China;
Department of PediatricsPeking University First HospitalBeijing China;
Department of PediatricsPeking University First HospitalBeijing China;
Bethlem myopathy; COL6A1; COL6A2; COL6A3; collagen VI; mosaicism; Ullrich congenital muscular dystrophy;
机译:中国胶原蛋白VI相关肌病患者群组遗传和临床调查结果
机译:中国人群综合征相关低丙基甲状腺功能亢进患者临床和遗传发现
机译:中国常染色体隐性纺纱术队患者群体的临床和遗传发现
机译:通过分级明智的深度多项式集合学习诊断遗传队列患者的帕金森氏病
机译:非霍奇金淋巴瘤的老年患者的白细胞生长因子的临床结果和成本效益:基于大量人群的研究结果。
机译:与MYH7相关的肌病:一组意大利患者的临床组织病理学和影像学发现
机译:大量患有ryanodine receptor 1基因相关性肌病的患者的临床和遗传学发现