Variability of epilepsy, autism, brachydactyly, and other clinical features in familial and sporadic 2q37.3 deletion

Antony E. Shrimpton, John A. Kessler, Lisa G. Shaffer, Cindy Stack, Ali Jalali, Robert Little, Joshua Goldstein, Brad Angle, Ajit Chary, Justine Coppinger, David J. Mathison, Sophia Khan, Andrew K. Poznanski, William B. Dobyns, David W. Craig, Joe J. Hoo, Dean Sarco, Alexander G. Bassuk*

*Corresponding author for this work

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Biochemistry, Genetics and Molecular Biology

Neuroscience

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