Wiszniewski, W., Hunter, J., Hanchard, N., Willer, J., Shaw, C., Tian, Q., . . . Lalani, S. (2013). TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.

Wiszniewski, W., et al. TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities. 2013.

Wiszniewski, W., et al. TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities. 2013.