Group by: Item Type | No Grouping Jump to: Article Number of items: 3. ArticleKaur, K. and Reddy, A.B.M. and Mukhopadhyay, A. and Mandal, A.K. and Hasnain, S.E. and Ray, K. and Thomas, R. and Balasubramanian, D. and Chakrabarti, S. (2005) Myocilin gene implicated in primary congenital glaucoma. Clinical Genetics, 67 (4). pp. 335-340. ISSN 0009-9163 Chakrabarti, S. and Kaur, K. and Sreelatha, K. and Acharya, M. and Devi, K.R. and Mukhopadhyay, A. and Mandal, A.K. and Hasnain, S.E. and Chandrasekhar, G. and Thomas, R. and Ray, K. (2005) Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India. Molecular Vision, 11. pp. 111-3. ISSN 1090-0535 Reddy, A.B.M. and Kaur, K. and Mandal, A.K. and Panicker, S.G. and Thomas, R. and Hasnain, S.E. and Balasubramanian, D. and Chakrabarti, S. (2004) Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients. Molecular vision, 10. pp. 696-702. ISSN 1090-0535
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