Eddie K. K. Ip
University of New South Wales
11 papers found
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CHDgene: A Curated Database for Congenital Heart Disease Genes
UploadHeterozygous loss of WBP11 function causes multiple congenital defects in humans and mice
Download from academic.oup.comdv-trio: a family-based variant calling pipeline using DeepVariant
Download from academic.oup.comVPOT: A Customizable Variant Prioritization Ordering Tool for Annotated Variants
Download from doi.orgNAD Deficiency, Congenital Malformations, and Niacin Supplementation
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