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.
Citace podle Chicago (17th ed.)Wiszniewski, W., et al. TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities. 2013.
Citace podle MLA (9th ed.)Wiszniewski, W., et al. TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities. 2013.
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