Publications
Export 2 results:
Filters: Author is Hurles, Matthew [Clear All Filters]
Integrating common and rare genetic variation in diverse human populations. Nature. 2010 ;467(7311):52-8.
. TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities. Am J Hum Genet. 2013 ;93(2):197-210.
.