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

Iris Schrijver

Showing results (1-10 of 97) with videos related to

Pageof 10
Sort By:
The Journal of Molecular Diagnostics : JMD|October 28, 2004
Hereditary non-syndromic sensorineural hearing loss: transforming silence to soundIris Schrijver
Clinical Chemistry|April 9, 2011
Mutation distribution in expanded screening for cystic fibrosis: making up the balance in a context of ethnic diversityIris Schrijver
Archives of Pathology & Laboratory Medicine|February 2, 2016
Pathology in the Medical Profession?: Taking the Pulse of Physician Wellness and BurnoutIris Schrijver
Expert Opinion on Medical Diagnostics|March 19, 2013
Inherited hearing loss: molecular genetics and diagnostic testingOana Vele, Iris Schrijver
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 13, 2011
Allelic discrimination of cis-trans relationships by digital polymerase chain reaction: GJB2 (p.V27I/p.E114G) and CFTR (p.R117H/5T)Neng Chen, Iris Schrijver
Expert Review of Molecular Diagnostics|May 19, 2006
Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysisIris Schrijver, Phyllis Gardner
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 19, 2016
A panoramic view of the accuracy of molecular genetic testingKaren E Weck, Iris Schrijver
Biochemical and Biophysical Research Communications|September 3, 2009
The digenic hypothesis unraveled: the GJB6 del(GJB6-D13S1830) mutation causes allele-specific loss of GJB2 expression in cisJuan Rodriguez-Paris, Iris Schrijver
Genes|April 9, 2014
Next generation DNA sequencing and the future of genomic medicineMatthew W Anderson, Iris Schrijver
Personalized Medicine|May 16, 2018
Between hype and hope: whole-genome sequencing in clinical medicineIris Schrijver, Stephen J Galli
Pageof 10

Showing results (1-10 of 97) with videos related to

Sort By:
Pageof 10
The Journal of Molecular Diagnostics : JMD|October 28, 2004
Hereditary non-syndromic sensorineural hearing loss: transforming silence to soundIris Schrijver
Clinical Chemistry|April 9, 2011
Mutation distribution in expanded screening for cystic fibrosis: making up the balance in a context of ethnic diversityIris Schrijver
Archives of Pathology & Laboratory Medicine|February 2, 2016
Pathology in the Medical Profession?: Taking the Pulse of Physician Wellness and BurnoutIris Schrijver
Expert Opinion on Medical Diagnostics|March 19, 2013
Inherited hearing loss: molecular genetics and diagnostic testingOana Vele, Iris Schrijver
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 13, 2011
Allelic discrimination of cis-trans relationships by digital polymerase chain reaction: GJB2 (p.V27I/p.E114G) and CFTR (p.R117H/5T)Neng Chen, Iris Schrijver
Expert Review of Molecular Diagnostics|May 19, 2006
Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysisIris Schrijver, Phyllis Gardner
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 19, 2016
A panoramic view of the accuracy of molecular genetic testingKaren E Weck, Iris Schrijver
Biochemical and Biophysical Research Communications|September 3, 2009
The digenic hypothesis unraveled: the GJB6 del(GJB6-D13S1830) mutation causes allele-specific loss of GJB2 expression in cisJuan Rodriguez-Paris, Iris Schrijver
Genes|April 9, 2014
Next generation DNA sequencing and the future of genomic medicineMatthew W Anderson, Iris Schrijver
Personalized Medicine|May 16, 2018
Between hype and hope: whole-genome sequencing in clinical medicineIris Schrijver, Stephen J Galli
Pageof 10