Cytogenetic abnormalities and fragile-x syndrome in Autism Spectrum Disorder

por Reddy, Kavita S
Publicado 2005

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

por Battu, Rajani, Jeyabalan, Nallathambi, Murthy, Praveen, Reddy, Kavita S, Schouten, Jan SAG, Webers, Caroll A
Publicado 2016

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

por Bandari, Aravind K., Muthusamy, Babylakshmi, Bhat, Sunil, Govindaraj, Periyasamy, Rajagopalan, Pavithra, Dalvi, Aparna, Shankar, Siddharth, Raja, Remya, Reddy, Kavita S., Madkaikar, Manisha, Pandey, Akhilesh
Publicado 2019

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

por Bandari, Aravind K., Bhat, Sunil, Archana, MV, Yadavalli, Sunita, Patel, Krishna, Rajagopalan, Pavithra, Madugundu, Anil K., Madkaikar, Manisha, Reddy, Kavita, Muthusamy, Babylakshmi, Pandey, Akhilesh
Publicado 2019

The criminogenic and psychological effects of police stops on adolescent black and Latino boys

por Del Toro, Juan, Lloyd, Tracey, Buchanan, Kim S., Robins, Summer Joi, Bencharit, Lucy Zhang, Smiedt, Meredith Gamson, Reddy, Kavita S., Pouget, Enrique Rodriguez, Kerrison, Erin M., Goff, Phillip Atiba
Publicado 2019

Surgery, Octreotide, Temozolomide, Bevacizumab, Radiotherapy, and Pegvisomant Treatment of an AIP Mutation‒Positive Child

por Dutta, Pinaki, Reddy, Kavita S, Rai, Ashutosh, Madugundu, Anil K, Solanki, Hitendra S, Bhansali, Anil, Radotra, Bishan D, Kumar, Narendra, Collier, David, Iacovazzo, Donato, Gupta, Prakamya, Raja, Remya, Gowda, Harsha, Pandey, Akhilesh, Devgun, Jagtar Singh, Korbonits, Márta
Publicado 2019