Spectrum of candidate gene mutations associated with Indian familial oculocutaneous and ocular albinism K Renugadevi, AK Sil, V Perumalsamy, P Sundaresan Molecular Vision 16, 1514, 2010 | 19 | 2010 |
Molecular Genetic Testing for Carrier-Prenatal Diagnosis and Computational Analysis of Oculocutaneous Albinism Type 1 K Renugadevi, JA Mary, V Perumalsamy, S Seshadri, S Jagadeesh, ... J Genet Disor Genet Rep 3, 2, 2014 | 4 | 2014 |
Cutaneous freckling: possible new clinical marker for the diagnosis of Hermansky-Pudlak syndrome in Indian Asian patients with oculocutaneous albinism K Arcot Sadagopan, R Kathirvel, RB Keep, P Sundaresan, H Huang, ... Ophthalmic Genetics 38 (2), 194-196, 2017 | 3 | 2017 |
Novel human pathological mutations. Gene symbol: OCA2. Disease: albinism, oculocutaneous II. K Renugadevi, AK Sil, V Perumalsamy, P Sundaresan Human Genetics 125 (3), 340-340, 2009 | 3 | 2009 |
Molecular genetic analysis and diagnosis of albinism patients in India K Renugadevi, AK Sil, P Vijayalakshmi, P Sundaresan JSM Genet Genomics 4, 2017 | 1 | 2017 |
Prenatal Molecular Diagnosis of Fetal Sample R Kathirvel, V Perumalsamy, AM John, S Rajaiah, S Jagadeesh, ... Investigative Ophthalmology & Visual Science 53 (14), 1579-1579, 2012 | | 2012 |
Genetic Carrier Screening for Oculocutaneous Albinism in India P Sundaresan, R Kathirvel, V Perumalsamy Investigative Ophthalmology & Visual Science 53 (14), 1560-1560, 2012 | | 2012 |
Novel Mutations in MC1R Gene: First Evidence for OCA Type II Disease in Indian Population R Kathirvel, SA Kumar, V Perumalsamy, S Periasamy Investigative Ophthalmology & Visual Science 52 (14), 3299-3299, 2011 | | 2011 |
Spectrum of Candidate Genes Mutation Associated with Indian Familial Oculocutaneous Albinism Patients P Sundaresan, K Renugadevi, AK Sil, P Vijayalakshmi Investigative Ophthalmology & Visual Science 51 (13), 2605-2605, 2010 | | 2010 |
Molecular genetics and functional analysis of albinism patients in India K Renugadevi Madurai, 0 | | |