R. Devi

Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea.

P. Vijayalakshmi, R. Devi, 2006, Molecular vision.

Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population.

P. Vijayalakshmi, R. Devi, C. Reena, 2005, Molecular vision.

Crystallin gene mutations in Indian families with inherited pediatric cataract

J. Hejtmancik, Y. Sergeev, Periasamy Sundaresan, 2008, Molecular vision.

Prevalence of methylene tetrahydrofolate reductase polymorphism in South Indian population

S. Naushad, R. Devi, V. Govindaiah, 2004 .

Triplet repeat polymorphism & fragile X syndrome in the Indian context.

V. Brahmachari, S. Srinath, R. Arthi, 1998, The Indian journal of medical research.

Plasma homocysteine levels correlated to interactions between folate status and methylene tetrahydrofolate reductase gene mutation in women with unexplained recurrent pregnancy loss

S. Naushad, A. Jyothy, K. S. Kumar, 2003, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

MTHFR (Ala 222 Val) polymorphism and AMI in patients with type II diabetes mellitus

W. Isabel, R. Aruna, R. Devi, 2009, Indian Journal of Clinical Biochemistry.