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

por Sharda, Sheetal, Panigrahi, Inusha, Marwaha, Ram Kumar
Publicado 2011

Autosomal Recessive Cutis Laxa Type II: Report of Novel Mutation in a Child

por Kumar, Rakesh, Sharda, Sheetal, Soni, Vimlesh, Nambiyar, Kaniyappan
Publicado 2017

Seven novel genetic variants in a North Indian cohort with classical homocystinuria

por Kaur, Rajdeep, Attri, Savita V., Saini, Arushi G., Sankhyan, Naveen, Singh, Satwinder, Faruq, Mohammed, Ramprasad, V. L., Sharda, Sheetal, Murugan, Sakthivel
Publicado 2020

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

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