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Response to Hall et al
Clinical exome sequencing vs. usual care for hereditary colorectal cancer diagnosis: A pilot comparative effectiveness study
Rare loss of function variants in candidate genes and risk of colorectal cancer
Actionable exomic incidental findings in 6503 participants: challenges of variant classification
Mutations in MYLPF Cause a Novel Segmental Amyoplasia that Manifests as Distal Arthrogryposis
Comparative effectiveness of next generation genomic sequencing for disease diagnosis: design of a randomized controlled trial in patients with colorectal cancer/polyposis syndromes
