Showing results 21 to 27 of 27
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Title | Author(s) | Issue Date | |
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Molecular Diagnosis for Paediatric Genetic Disorders Using Whole Exome Sequencing of the Next Generation Sequencing Technology Proceeding/Conference:Hong Kong Journal of Paediatrics (New series) | 2014 | ||
Monoallelic Mutations in CC2D1A Suggest a Novel Role in Human Heterotaxy and Ciliary Dysfunction Journal:Circulation: Genomic and Precision Medicine | 2020 | ||
Novel damaging mutations in CC2D1A suggest a role in human heterotaxy and ciliary dysfunction Proceeding/Conference:American Society of Human Genetics (ASHG) Virtual Meeting, 2020 | 2020 | ||
Policy-Based Primal-Dual Methods for Convex Constrained Markov Decision Processes Proceeding/Conference:The 37th AAAI Conference on Artificial Intelligence, AAAI 2023 (07/02/2023-14/02/2023, , , Washington, USA) | 7-Feb-2023 | ||
Prenatal Tobacco Exposure Shortens Telomere Length in Children Journal:Nicotine & Tobacco Research | 2017 | ||
PriVar: a toolkit for prioritizing SNVs and indels from next-generation sequencing data Journal:Bioinformatics | 2013 | ||
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