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Kym M Boycott
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researcher ORCID ID = 0000-0003-4186-8052
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Works
6
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.
scientific article
Homozygous mutations in MFN2 cause multiple symmetric lipomatosis associated with neuropathy
scientific article published on 17 June 2015
Unsolved recognizable patterns of human malformation: Challenges and opportunities
scientific article published on 01 December 2018
When One Diagnosis Is Not Enough
scientific article published on 7 December 2016
A novel multisystem disease associated with recessive mutations in the tyrosyl-tRNA synthetase (YARS) gene
scientific article published on 15 September 2016
The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model Organisms
scientific article published on 01 February 2020
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