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

R Z Hayeems

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Journal of Genetic Counseling|October 29, 2008
A systematic review of the effects of disclosing carrier results generated through newborn screeningR Z Hayeems, J P Bytautas, F A Miller
The British Journal of Ophthalmology|April 19, 2005
How patients experience progressive loss of visual function: a model of adjustment using qualitative methodsR Z Hayeems, G Geller, D Finkelstein, et al.
Journal of Genetic Counseling|August 12, 2015
Parents' Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic CounselingR Z Hayeems, R Babul-Hirji, N Hoang, et al.
Clinical Genetics|March 28, 2015
The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicineS C Bowdin, R Z Hayeems, N Monfared, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 1, 2019
The development of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE): a novel strategy for measuring the clinical utility of genetic testingR Z Hayeems, S Luca, W J Ungar, et al.
European Journal of Medical Genetics|December 4, 2018
Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatricsM J Szego, M S Meyn, C Shuman, et al.
Clinical Genetics|July 22, 2014
Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelinesJ A Anderson, R Z Hayeems, C Shuman, et al.
Public Health Genomics|September 25, 2009
Consent for newborn screening: the attitudes of health care providersF A Miller, R Z Hayeems, J C Carroll, et al.
Journal of Medical Ethics|November 27, 2016
Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?J A Anderson, M S Meyn, C Shuman, et al.
Journal of Medical Ethics|October 2, 2009
Clinical obligations and public health programmes: healthcare provider reasoning about managing the incidental results of newborn screeningF A Miller, R Z Hayeems, Y Bombard, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Journal of Genetic Counseling|October 29, 2008
A systematic review of the effects of disclosing carrier results generated through newborn screeningR Z Hayeems, J P Bytautas, F A Miller
The British Journal of Ophthalmology|April 19, 2005
How patients experience progressive loss of visual function: a model of adjustment using qualitative methodsR Z Hayeems, G Geller, D Finkelstein, et al.
Journal of Genetic Counseling|August 12, 2015
Parents' Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic CounselingR Z Hayeems, R Babul-Hirji, N Hoang, et al.
Clinical Genetics|March 28, 2015
The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicineS C Bowdin, R Z Hayeems, N Monfared, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 1, 2019
The development of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE): a novel strategy for measuring the clinical utility of genetic testingR Z Hayeems, S Luca, W J Ungar, et al.
European Journal of Medical Genetics|December 4, 2018
Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatricsM J Szego, M S Meyn, C Shuman, et al.
Clinical Genetics|July 22, 2014
Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelinesJ A Anderson, R Z Hayeems, C Shuman, et al.
Public Health Genomics|September 25, 2009
Consent for newborn screening: the attitudes of health care providersF A Miller, R Z Hayeems, J C Carroll, et al.
Journal of Medical Ethics|November 27, 2016
Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?J A Anderson, M S Meyn, C Shuman, et al.
Journal of Medical Ethics|October 2, 2009
Clinical obligations and public health programmes: healthcare provider reasoning about managing the incidental results of newborn screeningF A Miller, R Z Hayeems, Y Bombard, et al.
Pageof 2