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EFTA00287263
ing: screening of 572 individuals identifies high- penetrance mutations in cancer-susceptibility genes. Am J Hum Genet 2012;91:97-108. Saunders CJ, Miller NA, Soden SE, et al. Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. Sc! Trans! Med 2012;4(150):135-150.
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