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Number of items: 3.

Journal Article

Netravathi, Manjunath and Kumari, Renu and Kapoor, Saketh and Dakle, Pushkar and Dwivedi, Manish Kumar and Roy, Sumitabho Deb and Pandey, Paritosh and Saini, Jitender and Ramakrishna, Anil and Navalli, Devaraddi and Satishchandra, Parthasarathy and Pal, Pramod Kumar and Kumar, Arun and Faruq, Mohammed (2015) Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation. In: BMC MEDICAL GENETICS, 16 .

Kodaganur, Srinivas Gopinath and Kapoor, Saketh and Veerappa, Avinash M and Tontanahal, Sagar Jagannath and Sarda, Astha and Yathish, S and Prakash, Ravi D and Kumar, Arun (2013) Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature. In: Molecular Vision, 19 . pp. 1694-1706.

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.

This list was generated on Tue Jun 30 20:44:09 2015 IST.