机译:在Acromicicric和Geleophysic发育不良的视光盘肿胀
Department of Clinical GeneticsThe Children's Hospital at WestmeadSydney New South Wales Australia;
Department of OphthalmologyThe Children's Hospital at WestmeadSydney New South Wales Australia;
Department of Clinical GeneticsThe Children's Hospital at WestmeadSydney New South Wales Australia;
机译:在Acromicicric和Geleophysic发育不良的视光盘肿胀
机译:FBN1的TGFbeta结合蛋白样结构域5中的突变是造成肢端肥大症和凝胶体发育异常的原因。
机译:假性视乳头肿胀和视盘出血的儿童被误诊为视盘肿胀。
机译:光盘膨胀情况下2D彩色眼罩3D光神经头形状的深基于学习的估计
机译:视网膜层形状特征的光盘肿胀原因之间的差异
机译:用FBN1突变述评三种宫颈/凝胶物质发育不良三种案例
机译:导致Weill-Marchesani综合征的纤维蛋白1突变以及肢端和肢体发育异常会破坏硫酸乙酰肝素的相互作用。