Supplementary Data 1 for "A Novel Phenotype of 13q12.3 Microdeletion Characterized by Epilepsy in an Asian Child: A Case Report"
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资源简介：
The exome sequencing and single nucleotide polymorphism (SNP) array analysis of a 13q12.3 Microdeletion child.
创建时间：
2020-09-12
