MarfanSyndrome相关论文
FBN1 mutation in Chinese patients with Marfan syndrome and its gene diagnosis using haplotype linkag
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Identification of a novel lethal fibrillin-1 gene mutation in a Chinese Marfan family and correlatio
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目的 总结马凡综合征妊娠合并急性A型主动脉夹层的治疗经验.方法 3例患者的年龄25～31岁,平均28.6岁.妊娠32 ～ 38周,平均36.5周.手术......
目的评价台盼蓝及弹性虹膜拉钩在马凡综合征晶状体不全脱位手术中应用的效果。方法回顾性分析12例(17眼)马凡综合征晶状体不全脱位......
