Analysis of FOXD3 sequence variation in human ocular disease

Por Kloss, Bethany A. Volkmann, Reis, Linda M., Brémond-Gignac, Dominique, Glaser, Tom, Semina, Elena V.
Publicado em 2012

Exome Sequence Analysis of 14 Families With High Myopia

Por Kloss, Bethany A., Tompson, Stuart W., Whisenhunt, Kristina N., Quow, Krystina L., Huang, Samuel J., Pavelec, Derek M., Rosenberg, Thomas, Young, Terri L.
Publicado no Invest Ophthalmol Vis Sci (2017)

PITX2 and FOXC1 spectrum of mutations in ocular syndromes

Por Reis, Linda M, Tyler, Rebecca C, Volkmann Kloss, Bethany A, Schilter, Kala F, Levin, Alex V, Lowry, R Brian, Zwijnenburg, Petra J G, Stroh, Eliza, Broeckel, Ulrich, Murray, Jeffrey C, Semina, Elena V
Publicado em 2012

Trio-based exome sequencing arrests de novo mutations in early-onset high myopia

Por 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
Publicado no Proc Natl Acad Sci U S A (2017)