Search

Search Constraints

You searched for: Author/Creator Watkins, Nicholas

Search Results

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

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

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

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