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K. Renugadevi
K. Renugadevi
Thiagarajar College
Verified email at tcarts.in
Title
Cited by
Cited by
Year
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
192010
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
42014
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
32017
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
32009
Molecular genetic analysis and diagnosis of albinism patients in India
K Renugadevi, AK Sil, P Vijayalakshmi, P Sundaresan
JSM Genet Genomics 4, 2017
12017
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
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