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Filters: Author is Belmont, John W and Keyword is Base Sequence [Clear All Filters]
Replicative mechanisms for CNV formation are error prone. Nat Genet. 2013 ;45(11):1319-26.
. 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.
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