Kavita S Reddy

Genetic analysis and clinical phenotype of two Indian families with X-linked choroideremia

J. Schouten, P. Murthy, R. Battu, 2016, Indian journal of ophthalmology.

Sequencing of partial cypD gene for screening of Bifunctional Cytochrome P450 Monooxygenases from Bacillus cereus group

R. Prakasham, T. Sathish, P. Brahmaiah, 2010 .

Family-Based Next-Generation Sequencing Study Identifies an IL2RG Variant in an Infant with Primary Immunodeficiency

A. Pandey, A. Madugundu, Babylakshmi Muthusamy, 2019, Omics : a journal of integrative biology.

Next-Generation Sequencing Reveals Novel Mutations in X-linked Intellectual Disability.

A. Pandey, Babylakshmi Muthusamy, L. D. N. Selvan, 2017, Omics : a journal of integrative biology.

A Novel Splice Site Mutation in IFNGR2 in Patients With Primary Immunodeficiency Exhibiting Susceptibility to Mycobacterial Diseases

A. Pandey, Babylakshmi Muthusamy, P. Rajagopalan, 2019, Front. Immunol..