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3. Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomalies. (1st February 2022)

4. Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository. Issue 6 (19th April 2021)

5. Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiency. Issue 6 (1st October 2020)

8. Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study. Issue 4 (24th June 2020)