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S1R1C1
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Expanded newborn screening
Report
Probable benefits, harms and costs of expanding newborn screening
Independent response to House of Lords Science and Technology Committee Genomic Medicine report
Report
Predicting the risk of coronary heart disease with conventional, genetic and novel molecular biomarkers
Report
Tay Sachs Disease carrier screening in the Ashkenazi Jewish population
Report
Cell-free fetal nucleic acids for non-invasive prenatal diagnosis
Report
Evidence and evaluation: building public trust in genetic tests for common diseases
Report
Genetic ophthalmology in focus
Report
The evaluation of diagnostic laboratory tests and complex biomarkers
Report
The evaluation of clinical validity and clinical utility of genetic tests
Report
Family history as a risk factor for common, complex disease
Report
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S1R1C2
