Items where Author is "Dinesh, S. M."

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Number of items: 8.

Article

Avinash, M. V. and Suresh, R. V. and Sangeetha, V. and Kusuma, L. and Megha Murthy, and Dinesh, S. M. and Prakash, P. and Ramachandra, N. B. (2015) Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization. Genetics research, 97. pp. 1-12.

Dinesh, S. M. and Manu Prasad, and Avinash M. Veerappa, and Ramachandra, N. B. (2014) Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family. Genetics research, 96. pp. 1-10. ISSN 1469-5073

Veerappa, Avinash M. and Kusuma, L. and Sangeetha, V. and Megha, N. Murthy and Suresh, Raviraj V. and Ramachandra, N. B. and Dinesh, S. M. (2014) Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays. Genetics research, 96. pp. 1-12. ISSN 1469-5073

Dinesh, S. M. and Kusuma, L. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2011) GATA4 Specific Nonsynonymous Single-Nucleotide Polymorphisms in Congenital Heart Disease Patients of Mysore, India. GENETIC TESTING AND MOLECULAR BIOMARKERS, 15 (10). pp. 715-720.

Kusuma, L. and Dinesh, S. M. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2011) A Maiden Report on CRELD1 Single-Nucleotide Polymorphism Association in Congenital Heart Disease Patients of Mysore, South India. GENETIC TESTING AND MOLECULAR BIOMARKERS, 15 (7-8). pp. 483-487.

Kusuma, L. and Dinesh, S. M. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2011) Mutations of TFAP2B in congenital heart disease patients in Mysore, South India. Indian Journal of Medical Research, 134 (5). pp. 621-626. ISSN 0971-5916

Dinesh, S. M. and Kusuma, L. and Smitha, R. and Savitha, M. R. and Krishnamurthy, B. and Narayanappa, D. and Ramachandra, N. B. (2010) Single-Nucleotide Polymorphisms of NKX2.5 Found in Congenital Heart Disease Patients of Mysore, South India. GENETIC TESTING AND MOLECULAR BIOMARKERS, 14 (6). pp. 873-879.

Dinesh, S. M. and Karunakar, Prashantha and Amruthavalli, C. and Ramachandra, N. B. (2010) Analysis and Homology Modeling of Proteins Derived from NKX2.5 Non-synonymous Single Nucleotide Polymorphisms Involved in Congenital Heart Disease. Nature and Science, 8 (9).

This list was generated on Sat Sep 23 03:37:40 2017 IST.