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Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 12, 2019
Creating genetic reports that are understood by nonspecialists: a case studyGabriel Recchia, Antonia Chiappi, Gemma Chandratillake, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2019
Correction: Creating genetic reports that are understood by nonspecialists: a case studyGabriel Recchia, Antonia Chiappi, Gemma Chandratillake, et al.
European Journal of Human Genetics : EJHG|February 7, 2020
Recommendations for designing genetic test reports to be understood by patients and non-specialistsGeorge D Farmer, Harry Gray, Gemma Chandratillake, et al.
European Journal of Human Genetics : EJHG|October 14, 2025
Patient passports for rare diseases: results of a pilot studyJo Balfour, Vaila Morrison, Lydia Seed, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 4, 2013
Variant priorization and analysis incorporating problematic regions of the genomeAnil Patwardhan, Michael Clark, Alex Morgan, et al.
G3 (Bethesda, Md.)|November 5, 2015
Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome SequencingLorelei D Shoemaker, Michael J Clark, Anil Patwardhan, et al.
Genome Medicine|August 14, 2015
Achieving high-sensitivity for clinical applications using augmented exome sequencingAnil Patwardhan, Jason Harris, Nan Leng, et al.
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