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

L Bergstrom

Showing results (81-90 of 89) with videos related to

Pageof 9
Sort By:
You have reached the last page of results.This site can display upto 89 results.
Journal of Insurance Medicine (New York, N.Y.)|August 27, 2016
All-Cause Mortality for Diabetics or Individuals with Hyperglycemia Applying for Life InsuranceStephen A Freitas, Ross MacKenzie, David N Wylde, et al.
Proceedings. AMIA Symposium|February 5, 2002
A randomized controlled trial of the accuracy of clinical record retrieval using SNOMED-RT as compared with ICD9-CMP L Elkin, A P Ruggieri, S H Brown, et al.
Patient Education and Counseling|December 25, 2018
Agents of empathy: How medical interpreters bridge sociocultural gaps in genomic sequencing disclosures with Spanish-speaking familiesAmanda M Gutierrez, Emily E Statham, Jill O Robinson, et al.
Personalized Medicine|May 12, 2018
Portero versus portador: Spanish interpretation of genomic terminology during whole exome sequencing results disclosureAmanda M Gutierrez, Jill O Robinson, Emily E Statham, et al.
Scientific Reports|December 24, 2014
Social networks in primates: smart and tolerant species have more efficient networksCristian Pasquaretta, Marine Levé, Nicolas Claidière, et al.
American Journal of Human Genetics|September 26, 2017
Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic FeaturesPaweł Stankiewicz, Tahir N Khan, Przemyslaw Szafranski, et al.
The Journal of Clinical Investigation|October 4, 2017
Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like featuresRaphael Carapito, Martina Konantz, Catherine Paillard, 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.
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.
Pageof 9

Showing results (81-90 of 89) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 89 results.
Journal of Insurance Medicine (New York, N.Y.)|August 27, 2016
All-Cause Mortality for Diabetics or Individuals with Hyperglycemia Applying for Life InsuranceStephen A Freitas, Ross MacKenzie, David N Wylde, et al.
Proceedings. AMIA Symposium|February 5, 2002
A randomized controlled trial of the accuracy of clinical record retrieval using SNOMED-RT as compared with ICD9-CMP L Elkin, A P Ruggieri, S H Brown, et al.
Patient Education and Counseling|December 25, 2018
Agents of empathy: How medical interpreters bridge sociocultural gaps in genomic sequencing disclosures with Spanish-speaking familiesAmanda M Gutierrez, Emily E Statham, Jill O Robinson, et al.
Personalized Medicine|May 12, 2018
Portero versus portador: Spanish interpretation of genomic terminology during whole exome sequencing results disclosureAmanda M Gutierrez, Jill O Robinson, Emily E Statham, et al.
Scientific Reports|December 24, 2014
Social networks in primates: smart and tolerant species have more efficient networksCristian Pasquaretta, Marine Levé, Nicolas Claidière, et al.
American Journal of Human Genetics|September 26, 2017
Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic FeaturesPaweł Stankiewicz, Tahir N Khan, Przemyslaw Szafranski, et al.
The Journal of Clinical Investigation|October 4, 2017
Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like featuresRaphael Carapito, Martina Konantz, Catherine Paillard, 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.
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.
Pageof 9