Abhyankar, A., Lamendola‐Essel, M., Brennan, K., Giordano, J. L., Esteves, C., Felice, V., . . . Jobanputra, V. (2017). Clinical whole exome sequencing from dried blood spot identifies novel genetic defect underlying asparagine synthetase deficiency. Clin Case Rep.

Abhyankar, Avinash, Michelle Lamendola‐Essel, Kelly Brennan, Jessica L. Giordano, Cecilia Esteves, Vanessa Felice, Ronald Wapner, and Vaidehi Jobanputra. "Clinical Whole Exome Sequencing From Dried Blood Spot Identifies Novel Genetic Defect Underlying Asparagine Synthetase Deficiency." Clin Case Rep 2017.

Abhyankar, Avinash, et al. "Clinical Whole Exome Sequencing From Dried Blood Spot Identifies Novel Genetic Defect Underlying Asparagine Synthetase Deficiency." Clin Case Rep 2017.