Items where Author is "Smitha, R."

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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. ISSN 1945-0257

Smitha, R. and Savitha, M. R. and Krishnamurthy, Balasundaram and Doddaiah, Narayanappa and Prasanth, S. N. and Ramachandra, N. B. (2007) Association between pericentric inversion in chromosome 9 and congenital heart defects. International Journal of Human Genetics, 7 (3). pp. 241-248. ISSN 0972-3757

Malini, S. S. and Smitha, R. and Ramachandra, N. B. (2007) Evolution of phenylthiocarbamide taster trait in Mysore, South India. Indian Journal of Human Genetics, 13 (1). pp. 16-20. ISSN 1998-362X

Smitha, R. and Harshavardhan Gawde, M. and Hyderi, Abbas and Savitha, M. R. and Patel, Zareen M. and Krishnamurthy, Balasundaram and Ramachandra, N. B. (2006) De novo isochromosome 18p in a female dysmorphic child. Journal of Applied Genetics, 47 (4). pp. 397-401. ISSN 2190-3883

Smitha, R. and Ramachandra, N. B. (2006) Parental consanguinity increases congenital heart diseases in South India. Annals of Human Biology, 33 (5-6). pp. 519-528. ISSN 1464-5033

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