Study of a US cohort supports the role of ZNF644 and high-grade myopia susceptibility

Por Tran-Viet, Khanh-Nhat, St.Germain, Elizabeth, Soler, Vincent, Powell, Caldwell, Lim, Sing-Hui, Klemm, Thomas, Saw, Seang Mei, Young, Terri L.
Publicado em 2012

Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes

Por Tran-Viet, Khanh-Nhat, Soler, Vincent, Quiette, Valencia, Powell, Caldwell, Yanovitch, Tammy, Metlapally, Ravikanth, Luo, Xiaoyan, Katsanis, Nicholas, Nading, Erica, Young, Terri L.
Publicado em 2013

CYP1B1, MYOC, and LTBP2 Mutations in Primary Congenital Glaucoma Patients in the United States

Por LIM, SING-HUI, TRAN-VIET, KHANH-NHAT, YANOVITCH, TAMMY L., FREEDMAN, SHARON F., KLEMM, THOMAS, CALL, WHITNEY, POWELL, CALDWELL, RAVICHANDRAN, AJAY, METLAPALLY, RAVIKANTH, NADING, ERICA B., ROZEN, STEVE, YOUNG, TERRI L.
Publicado em 2012

Mutations in SCO2 Are Associated with Autosomal-Dominant High-Grade Myopia

Por Tran-Viet, Khanh-Nhat, Powell, Caldwell, Barathi, Veluchamy A., Klemm, Thomas, Maurer-Stroh, Sebastian, Limviphuvadh, Vachiranee, Soler, Vincent, Ho, Candice, Yanovitch, Tammy, Schneider, Georg, Li, Yi-Ju, Nading, Erica, Metlapally, Ravikanth, Saw, Seang-Mei, Goh, Liang, Rozen, Steve, Young, Terri L.
Publicado em 2013