We are a group of molecular biologists, geneticists, physicians, researchers and social workers who work in collaboration for the betterment of the patients and families with rare genetic disorders.

Our work plan includes to investigate and record complete clinical history of the genetically diseased patients, review available literature, to understand the possible causative genes in a case, and to develop a precise DNA test either by performing Sanger sequencing or via Next Generation Sequencing (NGS) tools including whole exome or candidate gene-panels sequencing. We have a thorough knowledge and experience of more than twenty years and are fully aware of the various modes of inheritances in human genetic disorders.

We aim

1. To educate and council families having genetic disorders by providing them efficient, accurate and cost effective molecular diagnostic tests and to reduce disease burden in their future generations by performing pre-marital testing.
2. To consult with the physicians and healthcare providers to decide possible management plans for patients with genetic disorders.
3. To train younger researchers from diverse backgrounds to excel in their career for their positive contribution in eridcation of the genetic disorders.