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Singh, Jaya and Mishra, Avshesh and Pandian, Arunachalam Jayamuruga and Mallipatna, Ashwin C and Khetan, Vikas and Sripriya, S and Kapoor, Suman and Agarwal, Smita and Sankaran, Satish and Katragadda, Shanmukh and Veeramachaneni, Vamsi and Hariharan, Ramesh and Subramanian, Kalyanasundaram and Mannan, Ashraf U (2016) Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort. In: MOLECULAR VISION, 22 . pp. 1036-1047.
Shah, Mohd Hussain and Bhat, Vishwanath and Shetty, Jyoti S and Kumar, Arun (2014) Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome. In: MOLECULAR VISION, 20 . pp. 790-796.
Kapoor, Saketh and Bindu, Parayil Sankaran and Taly, Arun B. and Sinha, Sanjib and Gayathri, Narayanappa and Rani, S. Vasantha and Chandak, Giriraj Ratan and Kumar, Arun (2012) Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy. In: MOLECULAR VISION, 18 (211-14). pp. 2022-2032.
