CURRICULUM VITAE NAME Shom Shanker Bhattacharya, PhD ...

80. The role of molecular genetics in the prenatal diagnosis of retinal dystrophies.
Evans K, Gregory C.Y., Fryer A, Whittaker J, Duvall-Young J, Bird A.C. and
Bhattacharya S.S. (1994). Eye. 9: 24-28.
81. Ocular findings associated with a three-base-pair deletion in the peripherin-
RDS gene in autosomal dominant Retinitis Pigmentosa. Wroblewski, J.J.,
Wells, J.A., Eckstein, A., Fitzke, F., Jubb, C., Keen, T.J., Inglehearn, C.F.,
Bhattacharya, S.S., Arden, G.B., Jay, M. and Bird, A.C. (1994). Br. J.
Ophthalmol. 78: 381-386.
82. Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with
autosomal dominant retinitis pigmentosa. Fuchs, S., Kranich, H, Denton,
M.J., Zrenner, E., Bhattacharya, S.S., Humphries, P. and Gal, A. (1994).
Hum. Mol. Genet. 3: 1203.
83. Retinitis pigmentosa families showing apparent X linked inheritance but
unlinked to the RP2 or RP3 loci. Aldred, M.A., Teague, P.W., Jay, M.,
Bundey, S., Redmond, R.M., Jay, B., Bird, A.C., Bhattacharya, S.S. and
Wright, A.F. (1994). J. Med. Genet. 31: 848-852.
84. Genetic heterogeneity in hereditary haemorrhagic telangiectasia. Porteous,
M.E., Curtis, A., Williams, O., Marchuk, D., Bhattacharya, S.S. and Burn, J.
(1994). J. Med. Genet. 31: 925-926.
85. Dinucleotide repeat polymorphism at the DXS977 locus. Yan, D., Wong, D.,
Zheng, K., Thiselton, D., Fujita, R., Sieving, P.A., Bhattacharya, S.S., Yang-
Feng, T.L., Richards, J.E. and Swaroop, A. (1994). Hum. Mol. Genet. 3:
1030.
86. Autosomal dominant macular dystrophy simulating North Carolina macular
dystrophy. Holz F.G., Evans K, Gregory C. Y., Bhattacharya S.S. and Bird A.C.
(1995). Arch. Ophthalmol. 113: 176-193.
87. Chromosome 19q cone-rod retinal dystrophy: ocular phenotype. Evans K Duvall-
Young J, Fitzke F, Arden G.B., Bhattacharya S.S. and Bird A.C. (1995). Arch.
Opthalmol. 113: 195-201.
88. Genetic Refinement of the chromosome 5q lattice corneal dystropy type I to
within two centimorgan interval. Gregory C.Y., Evans K, and Bhattacharya S.S.
(1995). J. Med. Genet. 32: 224-226.
89. Autosomal dominant pattern dystrophy of the retina associated with a 4-base
pair insertion at codon 140 in the peripherin/RDS gene. Kim, R.Y., Dollfus,
H., Keen, T.J., Fitzke, G.B., Arden, G.B., Bhattacharya, S.S. and Bird, A.C.
(1995) Arch. Ophthalmol. 113: 451-455.
90. Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits
variable expression. Kim, R.Y., Fitzke, F.W., Moore, A.T., Inglehearn, C.,
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