Browsing by Author Jia, Yanlei
Showing results 1 to 6 of 6
| Issue Date |
Title |
Author(s) |
| 2012 |
ABCB6 Mutations Cause Ocular Coloboma |
Wang, Lejing;He, Fei;Bu, Juan;Liu, Xiaqi;Du, Wei;Dong, Jiamei;Cooney, Jeffrey D.;Dubey, Sushi Kumar;Shi, Yi;Gong, Bo;Li, Jing;McBride, Paul F.;Jia, Yanlei;Lu, Fang;Soltis, Kathleen A.;Lin, Ying;Namburi, Prasanthi;Liang, Chen;Sundaresan, Periasamy;Paw, Barry H.;Li, Dean Y.;Phillips, John D.;Yang, Zhenglin |
| 2012 |
ABCB6 Mutations Cause Ocular Coloboma (vol 90, pg 40, 2012) |
Wang, Lejin;He, Fei;Bu, Juan;Zhen, Yuanli;Liu, Xiaoqi;Du, Wei;Dong, Jiamei;Cooney, Jeffrey D.;Dubey, Sushil Kumar;Shi, Yi;Gong, Bo;Li, Jing;McBride, Paul F.;Jia, Yanlei;Lu, Fang;Soltis, Kathleen A.;Lin, Ying;Namburi, Prasanthi;Liang, Chen;Sundaresan, Periasamy;Paw, Barry H.;Li, Wei;Li, Dean Y.;Phillips, John D.;Yang, Zhenglin |
| 2019 |
Modified Posterior Scleral Reinforcement as a Treatment for High Myopia in Children and Its Therapeutic Effect |
Miao, Zequn;Li, Luojia;Meng, Xiaoli;Guo, Lili;Cao, Di;Jia, Yanlei;He, Dongmei;Huang, Lvzhen;Wang, Lejin |
| 2012 |
A new novel mutation in FBN1 causes autosomal dominant Marfan syndrome in a Chinese family |
Dong, Jiamei;Bu, Juan;Du, Wei;Li, Yuan;Jia, Yanlei;Li, Jianchang;Meng, Xiaoli;Yuan, Minghui;Peng, Xiaojuan;Zhou, Aimin;Wang, Lejin |
| 2011 |
A novel frame-shift mutation in FRMD7 causes X-linked idiopathic congenital nystagmus in a Chinese family |
Du, Wei;Bu, Juan;Dong, Jiamei;Jia, Yanlei;Li, Jing;Liang, Chen;Si, Shancheng;Wang, Lejin |
| 2016 |
A previously unidentified deletion in G protein-coupled receptor 143 causing Xlinked congenital nystagrrtus in a Chinese family |
Liu, Jing;Jia, Yanlei;Wang, Lejin;Bu, Juan |
