SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE57859
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资源简介：
Array CGH analysis in order to determine the size of atypical NF1 deletions under investigation 12 atypical NF1 deletions were investigated with the custom array CGH
创建时间：
2014-08-28
