Items where Author is "Kusuma, L."

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Number of items: 7.

Article

Suresh, Raviraj V. and Kusuma, L. and Avinash, M. V. and Ramachandra, N. B. (2017) Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: a copy number variation approach. Indian Journal of Medical Research, 145 (1). pp. 39-50. ISSN 0975-9174

Suresh, R. V. and Narayannapa and Savitha and Ambika S. Udupa and Kusuma, L. and Sunil Kumar, P. and Ramachandra, N. B. (2017) Association of RFC1 A80G gene polymorphism with advanced maternal age in risk of Down syndrome. Current Medicine Research and Practice, 7 (1). 6 - 10. ISSN 2352-0817

Ramachandra, N. B. and Kusuma, L. (2015) An understanding of spinocerebellar ataxia. INDIAN JOURNAL OF MEDICAL RESEARCH, 141. pp. 148-150. ISSN 0971-5916

Avinash, M. V. and Sangeetha, V. and Kusuma, L. and Megha Murthy, N. and Raviraj, V. S. and Keshava, B. and Ramachandra, N. B. and Tejaswini, T. and Niveditha, B. Patel and Supriya Gowda, P. K. (2014) Insertion-deletions burden in copy number polymorphisms of the Tibetan population. Indian Journal of Human Genetics, 20 (2). pp. 166-174.

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 Bharath, A. Parshwanath and Savitha, R. M. and Balasundaram Krishnamurthy and Ramachandra, N. B. (2010) A rare case of congenital heart disease with ambiguous genitalia. Indian Journal of Human Genetics, 16 (3). pp. 166-168. ISSN 1998-362X

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

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