Browsing by Author Yong, V.H.K.

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Showing results 6 to 11 of 11 < previous 
Issue DateTitleAuthor(s)
2008Molecular analysis of CHX10 and MFRP in Chinese subjects with primary angle closure glaucoma and short axial length eyesAung, T. ; Lim, M.C.C.; Wong, T.T.L.; Yong, V.H.K.; Venkataraman, D.; Venkatraman, A.; Vithana, E.N. ; Chew, P.T.K. ; Thalamuthu, A.
2005Molecular analysis of the myocilin gene in Chinese subjects with chronic primary-angle closure glaucomaAung, T. ; Chew, P.T.K. ; Seah, S.K.L.; Gazzard, G.; Foster, P.J.; Yong, V.H.K.; Vithana, E.N.
Apr-2005Molecular analysis of the myocilin gene in Chinese subjects with chronic primary-angle closure glaucomaAung, T. ; Yong, V.H.K.; Chew, P.T.K. ; Seah, S.K.L.; Gazzard, G.; Foster, P.J.; Vithana, E.N.
2006Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)Vithana, E.N. ; Tan, D.T.H. ; Yong, V.H.K.; Morgan, P.; Casey, J.R.; Sundaresan, P.; Hemadevi, B.; Srinivasan, M.; Prajna, V.; Ebenezer, N.D.; Mohamed, M.D.; Inglehearn, C.F.; Anand, S.; Khine, K.O.; Khine, M.; Salto-Tellez, M. ; Guo, K.
2006Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)Vithana, E.N. ; Tan, D.T.H. ; Venkataraman, D.; Yong, V.H.K.; Aung, T. ; Morgan, P.; Casey, J.R.; Sundaresan, P.; Hemadevi, B.; Srinivasan, M.; Prajna, V.; Ebenezer, N.D.; Mohamed, M.D.; Inglehearn, C.F.; Anand, S.; Khine, K.O.; Salto-Tellez, M. ; Guo, K.
2009Surgical management and genetic analysis of a Chinese family with the S171P mutation in the UBIAD1 gene, the gene for Schnyder corneal dystrophyMehta, J.S.; Vithana, E.N. ; Venkataraman, D.; Venkatraman, A.; Yong, V.H.K.; Aung, T. ; Tan, D.T.H.