以下为句子列表：
英文: Conclusions A novel mutation of FBN gene with Glycine to Serine change is responsible for the ectopia lentis patients in a Chinese family.
中文: 论 FBN基因新突变G 0A (G S)是该家系单纯性晶状体异位的致病基因突变。
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英文: Isolated ectopia lentis (EL) is a rare autosomal dominant inherited eye disordercharacterized by stretching or disruption of the lenticular zonular filaments leads todisplacement of the lenses.
中文: 单纯性晶状体异位(isolated ectopia lentis,EL),是一种较为罕见的常染色体显性眼部疾病。 EL由晶状体悬韧带缺损或破裂引起悬挂力减弱所致,其临床特征是晶状体发生异位,并且呈双侧对称性发展。
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英文: Management of bilateral ectopia lentis et pupillae syndrome
中文: 双眼晶体异位并瞳孔综合症的治疗
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英文: Novel mutation of fibrillin gene cause ectopia lentis in a Chinese family
中文: 原纤维蛋白基因新突变导致单纯性晶状体异位
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英文: Screening and Analysis of Fibrillin- Gene (FBN) Mutation in a Chinese Family with Isolated Ectopia Lentis and Association Study of Schizophrenia and the Polymorphisms of COMT Gene in a Chinese Han Population
中文: 一个中国人单纯性晶状体异位家系FBN基因突变的研究以及中国汉族精神分裂症与COMT基因多态性的关联性分析
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