Five novel mutations of the FRMD7 gene in Chinese families with X-linked infantile nystagmus

por Li, Ningdong, Wang, Liming, Cui, Lihong, Zhang, Li, Dai, Suzhen, Li, Hongyan, Chen, Xia, Zhu, Lina, Hejtmancik, James F, Zhao, Kanxing
Publicado 2008

Characterization of novel RS1 exonic deletions in juvenile X-linked retinoschisis

por D’Souza, Leera, Cukras, Catherine, Antolik, Christian, Craig, Candice, Lee, Ji-Yun, He, Hong, Li, Shibo, Smaoui, Nizar, Hejtmancik, James F., Sieving, Paul A., Wang, Xinjing
Publicado 2013

EPHA2 Polymorphisms and Age-Related Cataract in India

por Sundaresan, Periasamy, Ravindran, Ravilla D., Vashist, Praveen, Shanker, Ashwini, Nitsch, Dorothea, Talwar, Badrinath, Maraini, Giovanni, Camparini, Monica, Nonyane, Bareng Aletta S., Smeeth, Liam, Chakravarthy, Usha, Hejtmancik, James F., Fletcher, Astrid E.
Publicado 2012