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You searched for: Author/Creator Robinson, John F.

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2. Characteristics of the Ontario Neurodegenerative Disease Research Initiative cohort. Issue 1 (30th March 2022)

3. Exome sequencing identifies NFS1 deficiency in a novel Fe‐S cluster disease, infantile mitochondrial complex II/III deficiency. Issue 1 (18th November 2013)

4. Genetic Variation in the Ontario Neurodegenerative Disease Research Initiative. (15th August 2019)

5. Identifying the Genetic Basis of Vascular Cognitive Impairment Using a Custom Designed Next-generation Sequencing-based Gene Panel. (June 2018)

6. Linkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxia. Issue 9 (24th July 2014)

7. Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically. Issue 12 (December 2016)

10. Targeted sequencing reveals expanded genetic diversity of human transfer RNAs. Issue 11 (2nd November 2019)