Ramachandran Ramya Devi

Summary

Affiliation: Aravind Eye Hospital
Country: India

Publications

  1. ncbi request reprint Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea
    Ramachandran Ramya Devi
    Department of Molecular Biology, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, Tamilnadu, India
    Mol Vis 12:190-5. 2006
  2. pmc Crystallin gene mutations in Indian families with inherited pediatric cataract
    Ramachandran Ramya Devi
    Department of Genetics, Dr G Venketaswamy Eye Research Institute, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, India
    Mol Vis 14:1157-70. 2008
  3. ncbi request reprint Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population
    Ramachandran Ramya Devi
    Department of Molecular Biology, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, Tamilnadu, India
    Mol Vis 11:846-52. 2005

Detail Information

Publications3

  1. ncbi request reprint Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea
    Ramachandran Ramya Devi
    Department of Molecular Biology, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, Tamilnadu, India
    Mol Vis 12:190-5. 2006
    ....
  2. pmc Crystallin gene mutations in Indian families with inherited pediatric cataract
    Ramachandran Ramya Devi
    Department of Genetics, Dr G Venketaswamy Eye Research Institute, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, India
    Mol Vis 14:1157-70. 2008
    ..This study is aimed at identification of the spectrum and frequency of crystallin gene mutations in cataractous patients in an Indian population...
  3. ncbi request reprint Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population
    Ramachandran Ramya Devi
    Department of Molecular Biology, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai, Tamilnadu, India
    Mol Vis 11:846-52. 2005
    ..The present study aimed to identify the spectrum of mutations in Connexin 46 in the Indian population...