Assessing Utility of Clinical Exome Sequencing in Diagnosis of Rare Idiopathic Neurodevelopmental Disorders in Indian Population von Sheth, Harsh, Pancholi, Dhairya, Bhavsar, Riddhi, Mannan, Ashraf, Ganapathy, Aparna, Chowdhury, Mayank, Shah, Sudhir, Solanki, Dhawal, Sheth, Frenny, Sheth, Jayesh

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