Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Clara Gaff

Showing results (91-100 of 109) with videos related to

Pageof 11
Sort By:
BMJ Paediatrics Open|April 12, 2018
A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohortLilian Downie, Jane L Halliday, Rachel A Burt, et al.
European Journal of Human Genetics : EJHG|December 13, 2019
Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
Genome Medicine|July 29, 2015
Cpipe: a shared variant detection pipeline designed for diagnostic settingsSimon P Sadedin, Harriet Dashnow, Paul A James, et al.
European Journal of Human Genetics : EJHG|November 10, 2020
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
Internal Medicine Journal|April 3, 2018
Exploring the feasibility and utility of exome-scale tumour sequencing in a clinical settingBelinda Lee, Ben Tran, Arthur L Hsu, et al.
Plos One|November 8, 2021
Return of individual research results from genomic research: A systematic review of stakeholder perspectivesDanya F Vears, Joel T Minion, Stephanie J Roberts, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 16, 2024
Offering complex genomic screening in acute pediatric settings: Family decision-making and outcomesMelissa Martyn, Ling Lee, Alli Jan, et al.
NPJ Genomic Medicine|August 1, 2018
Responsible sharing of biomedical data and biospecimens via the "Automatable Discovery and Access Matrix" (ADA-M)J Patrick Woolley, Emily Kirby, Josh Leslie, et al.
Haematologica|February 15, 2020
Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromesPiers Blombery, Lucy Fox, Georgina L Ryland, et al.
Haematologica|April 2, 2024
<i>Erratum</i> to: Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromesPiers Blombery, Lucy Fox, Georgina L Ryland, et al.
Pageof 11

Showing results (91-100 of 109) with videos related to

Sort By:
Pageof 11
BMJ Paediatrics Open|April 12, 2018
A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohortLilian Downie, Jane L Halliday, Rachel A Burt, et al.
European Journal of Human Genetics : EJHG|December 13, 2019
Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
Genome Medicine|July 29, 2015
Cpipe: a shared variant detection pipeline designed for diagnostic settingsSimon P Sadedin, Harriet Dashnow, Paul A James, et al.
European Journal of Human Genetics : EJHG|November 10, 2020
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
Internal Medicine Journal|April 3, 2018
Exploring the feasibility and utility of exome-scale tumour sequencing in a clinical settingBelinda Lee, Ben Tran, Arthur L Hsu, et al.
Plos One|November 8, 2021
Return of individual research results from genomic research: A systematic review of stakeholder perspectivesDanya F Vears, Joel T Minion, Stephanie J Roberts, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 16, 2024
Offering complex genomic screening in acute pediatric settings: Family decision-making and outcomesMelissa Martyn, Ling Lee, Alli Jan, et al.
NPJ Genomic Medicine|August 1, 2018
Responsible sharing of biomedical data and biospecimens via the "Automatable Discovery and Access Matrix" (ADA-M)J Patrick Woolley, Emily Kirby, Josh Leslie, et al.
Haematologica|February 15, 2020
Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromesPiers Blombery, Lucy Fox, Georgina L Ryland, et al.
Haematologica|April 2, 2024
<i>Erratum</i> to: Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromesPiers Blombery, Lucy Fox, Georgina L Ryland, et al.
Pageof 11