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

Wybo Dondorp

Showing results (41-50 of 55) with videos related to

Pageof 6
Sort By:
BMC Medical Ethics|November 11, 2023
Uncertain futures and unsolicited findings in pediatric genomic sequencing: guidelines for return of results in cases of developmental delayCandice Cornelis, Wybo Dondorp, Ineke Bolt, et al.
Human Reproduction (Oxford, England)|January 17, 2014
Beyond the dichotomy: a tool for distinguishing between experimental, innovative and established treatmentVeerle Provoost, Kelly Tilleman, Arianna D'Angelo, et al.
Human Reproduction Update|March 8, 2013
Dynamics and ethics of comprehensive preimplantation genetic testing: a review of the challengesKristien Hens, Wybo Dondorp, Alan H Handyside, et al.
European Journal of Human Genetics : EJHG|July 28, 2016
Whole-exome sequencing in pediatrics: parents' considerations toward return of unsolicited findings for their childCandice Cornelis, Aad Tibben, Wybo Dondorp, et al.
European Journal of Human Genetics : EJHG|June 6, 2023
Consanguineous couples' experiences and views regarding expanded carrier screening: Barriers and facilitators in the decision-making processSanne van der Hout, Anke J Woudstra, Wybo Dondorp, et al.
Prenatal Diagnosis|June 5, 2023
The influence of the introduction of a national prenatal screening program on late termination of pregnancy, a retrospective cohort studyJudith Horenblas, Jana de Vries, Charlotte Jansen, et al.
Prenatal Diagnosis|June 23, 2022
Views of patients and parents of children with genetic disorders on population-based expanded carrier screeningAnke J Woudstra, Lieke M van den Heuvel, Elsbeth H van Vliet-Lachotzki, et al.
Plos One|February 20, 2020
Situating trade-offs: Stakeholder perspectives on overtreatment versus missed diagnosis in transition to Xpert MTB/RIF Ultra in Kenya and SwazilandMuthoni Mwaura, Kekeletso Kao, Jesse Wambugu, et al.
Family Practice|February 1, 2023
Primary care professionals' views on population-based expanded carrier screening: an online focus group studyLieke M van den Heuvel, Anke J Woudstra, Sanne van der Hout, et al.
European Journal of Human Genetics : EJHG|January 13, 2018
Responsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHREGuido De Wert, Björn Heindryckx, Guido Pennings, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
BMC Medical Ethics|November 11, 2023
Uncertain futures and unsolicited findings in pediatric genomic sequencing: guidelines for return of results in cases of developmental delayCandice Cornelis, Wybo Dondorp, Ineke Bolt, et al.
Human Reproduction (Oxford, England)|January 17, 2014
Beyond the dichotomy: a tool for distinguishing between experimental, innovative and established treatmentVeerle Provoost, Kelly Tilleman, Arianna D'Angelo, et al.
Human Reproduction Update|March 8, 2013
Dynamics and ethics of comprehensive preimplantation genetic testing: a review of the challengesKristien Hens, Wybo Dondorp, Alan H Handyside, et al.
European Journal of Human Genetics : EJHG|July 28, 2016
Whole-exome sequencing in pediatrics: parents' considerations toward return of unsolicited findings for their childCandice Cornelis, Aad Tibben, Wybo Dondorp, et al.
European Journal of Human Genetics : EJHG|June 6, 2023
Consanguineous couples' experiences and views regarding expanded carrier screening: Barriers and facilitators in the decision-making processSanne van der Hout, Anke J Woudstra, Wybo Dondorp, et al.
Prenatal Diagnosis|June 5, 2023
The influence of the introduction of a national prenatal screening program on late termination of pregnancy, a retrospective cohort studyJudith Horenblas, Jana de Vries, Charlotte Jansen, et al.
Prenatal Diagnosis|June 23, 2022
Views of patients and parents of children with genetic disorders on population-based expanded carrier screeningAnke J Woudstra, Lieke M van den Heuvel, Elsbeth H van Vliet-Lachotzki, et al.
Plos One|February 20, 2020
Situating trade-offs: Stakeholder perspectives on overtreatment versus missed diagnosis in transition to Xpert MTB/RIF Ultra in Kenya and SwazilandMuthoni Mwaura, Kekeletso Kao, Jesse Wambugu, et al.
Family Practice|February 1, 2023
Primary care professionals' views on population-based expanded carrier screening: an online focus group studyLieke M van den Heuvel, Anke J Woudstra, Sanne van der Hout, et al.
European Journal of Human Genetics : EJHG|January 13, 2018
Responsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHREGuido De Wert, Björn Heindryckx, Guido Pennings, et al.
Pageof 6