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

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

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

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

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

par 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.
Publié 2012

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

par 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.
Publié 2013