High prevalence of relapse in children with Philadelphia-like acute lymphoblastic leukemia despite risk-adapted treatment
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A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES data
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Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests
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Genetics and Insurance in Australia: Concerns around a Self-Regulated Industry
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Genomics in healthcare: GA4GH looks to 2022
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