| 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 |
| Apr-2020 |
The efficacy of modified posterior scleral reinforcement with round scleral patches in Chinese children with high myopia |
Dong, Xuran;Liu, Jing;Bu, Juan |
| 2017 |
A Gene Scan Study of RPE65 in Chinese Patients with Leber Congenital Amaurosis |
Liu, Jing;Bu, Juan |
| 2008 |
Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese family |
Zhang, Shirong;Liu, Mugen;Dong, Jia Mei;Yin, Ke;Wang, Pengyun;Bu, Juan;Li, Jing;Hao, Yan Sheng;Hao, Ping;Wang, Qing Kenneth;Wang, Lejin |
| Dec-2022 |
Learning from inbound foreign acquisitions for outbound expansion by emerging market MNEs |
Bu, Juan;Tang, Yinuo;Luo, Yadong;Li, Chengguang |
| 2017 |
A Modified Amblyopia Treatment Index in Beijing, China: Lessons Learned |
Galvin, Jennifer Ann;Bu, Juan;Li, Wendy F. |
| 2017 |
A Modified Amblyopia Treatment Index in Beijing, China: Lessons Learned |
Galvin, Jennifer Ann;Bu, Juan;Li, Wendy F. |
| 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 novel splice donor site mutation in EPHA2 caused congenital cataract in a Chinese family |
Bu, Juan;He, Sijie;Wang, Lejin;Li, Jiankang;Liu, Jing;Zhang, Xiuqing |
| 2017 |
Parental Perspectives on Myopia in Beijing, China |
Li, Wendy F.;Bu, Juan;Warren, Joshua L.;Teng, Christopher |
| 2017 |
Parental Perspectives on Myopia in Beijing, China |
Li, Wendy F.;Bu, Juan;Warren, Joshua L.;Teng, Christopher |
| 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 |
| Feb-2021 |
Response to letter "The impact of scleral buckling technique application in diminishing high myopia" |
Dong, Xuran;Liu, Jing;Bu, Juan |
