机译:恶性双侧嗜铬细胞瘤家族中VHL基因的突变筛选:从孤立的家族性嗜铬细胞瘤到von Hippel-Lindau病
Endocrinology and Metabolism Research Centre Shariati Hospital Tehran University of Medical Sciences Fifth floor North Kargar Ave 14114 Tehran Iran;
Endocrinology and Metabolism Research Centre Shariati Hospital Tehran University of Medical Sciences Fifth floor North Kargar Ave 14114 Tehran Iran;
Endocrinology and Metabolism Research Centre Shariati Hospital Tehran University of Medical Sciences Fifth floor North Kargar Ave 14114 Tehran Iran;
Endocrinology and Metabolism Research Centre Shariati Hospital Tehran University of Medical Sciences Fifth floor North Kargar Ave 14114 Tehran Iran;
Endocrinology and Metabolism Research Centre Shariati Hospital Tehran University of Medical Sciences Fifth floor North Kargar Ave 14114 Tehran Iran;
Endocrinology and Metabolism Research Centre Shariati Hospital Tehran University of Medical Sciences Fifth floor North Kargar Ave 14114 Tehran Iran;
Endocrinology and Metabolism Research Centre Shariati Hospital Tehran University of Medical Sciences Fifth floor North Kargar Ave 14114 Tehran Iran;
Familial pheochromocytoma; von Hippel-Lindau disease; Mutation; Pheochromocytomas;
机译:患有恶性双侧嗜铬细胞瘤的家庭中VHL基因的突变筛选:从孤立的家族性嗜铬细胞瘤到von Hippel-Lindau病。
机译:von Hippel-Lindau(VHL)种系突变V84L表现为早期发作的双侧嗜铬细胞瘤。
机译:非综合征性嗜铬细胞瘤中von Hippel-Lindau基因突变的遗传筛查:低流行和假阳性或误诊表明需要谨慎
机译:Von Hippel-Lindau(VHL)基因缺陷对人类肾脏的影响
机译:p.Arg82Leu von Hippel-Lindau(VHL)基因突变在印度家族性双边嗜铬细胞瘤的一个家庭的三个成员中:分子分析和计算机模拟
机译:p.arg82Leu von Hippel-Lindau(VHL)基因突变在印度家族性双侧嗜铬细胞瘤家族的三个成员中:分子分析和计算机表征。