Associated Papers
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Targeted next generation sequencing as a tool for precision medicine.
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Supplement: 12920_2019_527_MOESM1_ESM.xlsx › Table_S6
Polymorphisms of SLC22A9 (hOAT7) in Korean Females with Osteoporosis.
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De novo mutations in moderate or severe intellectual disability.
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Plos Genetics, 2014
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