MOMO Syndrome with Holoprosencephaly and Cryptorchidism: Expanding the Spectrum of the New Obesity Syndrome

by Sheetal Sharda, Inusha Panigrahi, Ram Kumar Marwaha
Published 2011-01-01

Autosomal recessive cutis laxa Type II: Report of novel mutation in a child

by Rakesh Kumar, Sheetal Sharda, Vimlesh Soni, Kaniyappan Nambiyar
Published 2017-01-01

P717: The landscape of clinical geneticists’ perspectives and practices in India

by Sushma Patil, Udhaya Kotecha, Sheetal Sharda, Parth Shah, Nidhi Shah
Published 2024-01-01

P472: Exploring diagnostic yield and challenges in exome sequencing in highly consanguineous Tamil Nadu cohort from South India*

by Nivedita Rajakumar, Manaswini Krishnakumar, Udhaya Kotecha, Priya Ranganath, Ashka Prajapati, Rema Chandramohan, Anuradha D, Kalpana MS, Annie Pradeepa, Sheetal Sharda, Parth Shah, Nidhi Shah
Published 2024-01-01

NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results – a pilot study

by Kanika Singh, Sunita Bijarnia-Mahay, V. L. Ramprasad, Ratna Dua Puri, Sandhya Nair, Sheetal Sharda, Renu Saxena, Sudha Kohli, Samarth Kulshreshtha, Indrani Ganguli, Kanwal Gujral, Ishwar C. Verma
Published 2020-11-01