PITX2 and FOXC1 spectrum of mutations in ocular syndromes by REIS, Linda M, TYLER, Rebecca C, SEMINA, Elena V, KLOSS, Bethany A.volkmann, SCHILTER, Kala F, LEVIN, Alex V, LOWRY, R. Brian, ZWIJNENBURG, Petra Jg, STROH, Eliza, BROECKEL, Ulrich, MURRAY, Jeffrey C

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Trio-based exome sequencing arrests de novo mutations in early-onset high myopia by Jin, Zi-Bing, Wu, Jinyu, Huang, Xiu-Feng, Feng, Chun-Yun, Cai, Xue-Bi, Mao, Jian-Yang, Xiang, Lue, Wu, Kun-Chao, Xiao, Xueshan, Kloss, Bethany A., Li, Zhongshan, Liu, Zhenwei, Huang, Shenghai, Shen, Meixiao, Cheng, Fei-Fei, Cheng, Xue-Wen, Zheng, Zhi-Li, Chen, Xuejiao, Zhuang, Wenjuan, Zhang, Qingjiong, Young, Terri L., Xie, Ting, Lu, Fan, Qu, Jia

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Exome Sequence Analysis of 14 Families With High Myopia by Kloss, Bethany A, Tompson, Stuart W, Whisenhunt, Kristina N, Quow, Krystina L, Huang, Samuel J, Pavelec, Derek M, Rosenberg, Thomas, Young, Terri L

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Analysis of FOXD3 sequence variation in human ocular disease by Kloss, Bethany A Volkmann, Reis, Linda M, Brémond-Gignac, Dominique, Glaser, Tom, Semina, Elena V

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Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity by Souma, Tomokazu, Tompson, Stuart W, Thomson, Benjamin R, Siggs, Owen M, Kizhatil, Krishnakumar, Yamaguchi, Shinji, Feng, Liang, Limviphuvadh, Vachiranee, Whisenhunt, Kristina N, Maurer-Stroh, Sebastian, Yanovitch, Tammy L, Kalaydjieva, Luba, Azmanov, Dimitar N, Finzi, Simone, Mauri, Lucia, Javadiyan, Shahrbanou, Souzeau, Emmanuelle, Zhou, Tiger, Hewitt, Alex W, Kloss, Bethany, Burdon, Kathryn P, Mackey, David A, Allen, Keri F, Ruddle, Jonathan B, Lim, Sing-Hui, Rozen, Steve, Tran-Viet, Khanh-Nhat, Liu, Xiaorong, John, Simon, Wiggs, Janey L, Pasutto, Francesca, Craig, Jamie E, Jin, Jing, Quaggin, Susan E, Young, Terri L

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