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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 6, 2018
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite studyM Ragan Hart, Barbara B Biesecker, Carrie L Blout, et al.
Nature Genetics|October 19, 2021
Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidenceSarah Moody, Sergey Senkin, S M Ashiqul Islam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 24, 2019
Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite studyM Ragan Hart, Barbara B Biesecker, Carrie L Blout, et al.
American Journal of Medical Genetics. Part A|August 26, 2021
Expanding the phenotype of ASXL3-related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3Schaida Schirwani, Shadi Albaba, Deanna Alexis Carere, et al.
Nature|April 23, 2025
Geographic and age variations in mutational processes in colorectal cancerMarcos Díaz-Gay, Wellington Dos Santos, Sarah Moody, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Geographic and age-related variations in mutational processes in colorectal cancerMarcos Díaz-Gay, Wellington Dos Santos, Sarah Moody, et al.
Biorxiv : the Preprint Server for Biology|February 12, 2026
A searchable metadata network graph for microbiome metabolomicsVincent Charron-Lamoureux, Shipei Xing, Abubaker Patan, et al.
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