Publications

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Filters: Author is Glass, Ian A and Keyword is High-Throughput Nucleotide Sequencing  [Clear All Filters]
2016
Bi W, Glass IA, Muzny DM, Gibbs RA, Eng CM, Yang Y, Sun A. Whole exome sequencing identifies the first STRADA point mutation in a patient with polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome (PMSE). Am J Med Genet A. 2016 ;170(8):2181-5.