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ARVO Annual Meeting Abstract May 2006

Phenotypic Characterization and Mutation Analysis of Peripapillary Pigmentary Retinal Dystrophy Patients

K.Y. Lee; A.H. C. Koh; T. Aung; V.H. K. Yong; E.N. Vithana

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):1703.

ARVO Annual Meeting Abstract May 2006

The Identification and Characterization of the Gene Responsible for Autosomal Recessive Congenital Hereditary Endothelial Dystrophy (CHED2) on 20p13

E.N. Vithana; C. Inglehearn; N. Ebenezer; P. Sundaresan; M. Srinivasan; M.D. Mohamed; K.O. Khine; M.M. Khine; D. Tan; T. Aung

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):2295.

ARVO Annual Meeting Abstract May 2006

IL1 Gene Cluster Polymorphisms and Risk for Primary Open Angle Glaucoma in Chinese Patients

T. Aung; A.C. S. How; X.–Y. Chew; V.H. K. Yong; M.C. C. Lim; K.Y. C. Lee; E.N. Vithana

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):184.

ARVO Annual Meeting Abstract May 2005

Molecular Analysis of the Myocilin Gene in Chinese Subjects With Chronic Primary Angle Closure Glaucoma

T. Aung; V.H. K. Yong; P.T. K. Chew; S.K. L. Seah; G. Gazzard; P.J. Foster; E.N. Vithana

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):31.

ARVO Annual Meeting Abstract May 2005

Lack of Association of IVS8+4 C/T and IVS8+32 T/C Polymorphisms in the OPA1 Gene With Normal Tension Glaucoma in Patients From Singapore, India and Japan

G. Kumaramanickavel; T. Aung; S. Sripriya; N. Waseem; K. Okada; S.K. L. Seah; M. Baskaran; H.K. Mishima; E.N. Vithana; S. Bhattacharya

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):3811.

ARVO Annual Meeting Abstract May 2005

Identification of the Genetic Basis of Partial Penetrance Phenotype of RP11 Locus (PRPF31) on Chromosome 19q13.4

B. Ghosh; C. Charakova; E.N. Vithana; S.S. Bhattacharya

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):3831.

ARVO Annual Meeting Abstract May 2005

Analysis of Known Corneal Endothelial Dystrophy Loci in a Chinese Family With Fuchs Endothelial Dystrophy

A.C. S. How; T. Aung; V.H. K. Yong; D.T. H. Tan; E.N. Vithana

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):4933.

ARVO Annual Meeting Abstract May 2005

Characterization of Bietti's Crystalline Dystrophy Patients With CYP4V2 Mutations

K.Y. C. Lee; A.H. C. Koh; T. Aung; V.H. K. Yong; A.M. Y. Fong; C.L. Ang; E.N. Vithana

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):1841.

ARVO Annual Meeting Abstract May 2004

Can the stability of a mutant mRNA copy of PRPF31 with an 11bp deletion be compromised through alternative splicing?

E.N. Vithana; C. Chakarova; R.J. Patel; S.S. Bhattacharya

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):2484.

ARVO Annual Meeting Abstract May 2003

Autosomal Dominant Retinitis Pigmentosa Mapped on Chromosome 19q (adRP19q): Phenotype, Electrophysiology Tests and Genetic Counselling

L. Pelosini; N. Lansel; L. Winchester; R.B. Dilmaghani; G. Holder; E.N. Vithana; S.S. Bhattacharya; A.C. Bird

Invest. Ophthalmol. Vis. Sci.. 2003; 44(13):528.

ARVO Annual Meeting Abstract May 2003

Expression of Precursor RNA Processing Factor 31 (PRPF31) mRNA in Patients with Autosomal Dominant Retinitis Pigmentosa: A Molecular `Clue' for Incomplete Penetrance?

E.N. Vithana; L. Abu-Safieh; A.C. Bird; D.M. Hunt; S.A. Bustin; S.S. Bhattacharya

Invest. Ophthalmol. Vis. Sci.. 2003; 44(13):2018.

ARVO Annual Meeting Abstract May 2003

Functional Studies of Mutations in HPRP3 Associated with Autosomal Dominant Retinitis Pigmentosa

C.F. Chakarova; E.N. Vithana; S. Wilkie; D.M. Hunt; S.S. Bhattacharya

Invest. Ophthalmol. Vis. Sci.. 2003; 44(13):2838.

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