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Filters: Author is Belmont, John W and Keyword is Genetic Variation [Clear All Filters]
Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy. Am J Hum Genet. 2016 ;98(3):562-570.
. . Replicative mechanisms for CNV formation are error prone. Nat Genet. 2013 ;45(11):1319-26.
. Clan genomics and the complex architecture of human disease. Cell. 2011 ;147(1):32-43.
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