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22. A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation of Tian G; Cristancho AG; Dubbs HA; Liu GT; Cowan NJ; Goldberg EM Mol Genet Genomic Med; 2016 Nov; 4(6):599-603. PubMed ID: 27896282 [TBL] [Abstract][Full Text] [Related]
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