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Panicker SG 2

Showing records 1 to 2 | Display all abstracts from Panicker SG

9719 Identification of R368H as a predominant CYP1B1 allele causing primary congenital glaucoma in Indian patients
Reddy AB; Panicker SG; Mandal AK; Hasnain SE; Balasubramanian D
Investigative Ophthalmology and Visual Science 2003; 44: 4200-4203

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9820 PAX6 gene mutations and genotype-phenotype correlations in sporadic cases of aniridia from India
Dharmaraj N; Reddy ABM; Kiran VS; Mandal AK; Panicker SG; Chakrabarti S
Ophthalmic Genetics 2003; 24: 161-165

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