Refining the Phenotype Associated with GNB1 Mutations: Clinical Data on 18 Newly Identified Patients and Review of the Literature
Vinodh Narayanan, Nancy J Mendelsohn, Ana Bircher, Tristan T Sands, Alejandro Iglesias, American Journal of Medical Genetics Part ADe Novo Variant in KIF26B Is Associated with Pontocerebellar Hypoplasia with Infantile Spinal Muscular Atrophy
Pankaj B Agrawal, Vinodh Narayanan, Monica H Wojcik, Sanjay P Prabhu, American Journal of Medical Genetics Part AA Novel FBXO28 Frameshift Mutation in a Child with Developmental Delay, Dysmorphic Features, and Intractable Epilepsy: A Second Gene That May Contribute to the 1q41‐q4...
Vinodh Narayanan, Newell Belnap, American Journal of Medical Genetics Part A
