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

Karin M Dent

Showing results (11-20 of 18) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 18 results.
American Journal of Medical Genetics. Part A|April 26, 2012
Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harmsHolly K Tabor, Jacquie Stock, Tracy Brazg, et al.
American Journal of Medical Genetics. Part A|April 24, 2013
Practices and policies of clinical exome sequencing providers: analysis and implicationsSeema M Jamal, Joon-Ho Yu, Jessica X Chong, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 3, 2004
Methodology of a multistate study of congenital hearing loss: preliminary data from Utah newborn screeningKarin M Dent, Aileen Kenneson, Janice C Palumbos, et al.
Journal of Genetic Counseling|May 7, 2025
Genetic counseling program director competencies as proposed by the program leadership development subcommittee of the Genetic Counselor Educators AssociationMonica L Marvin, Dawn C Allain, Erin P Carmany, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2016
My46: a Web-based tool for self-guided management of genomic test results in research and clinical settingsHolly K Tabor, Seema M Jamal, Joon-Ho Yu, et al.
American Journal of Medical Genetics. Part A|January 19, 2020
Novel KIAA1033/WASHC4 mutations in three patients with syndromic intellectual disability and a review of the literatureMirna Assoum, Ange-Line Bruel, Melissa L Crenshaw, et al.
American Journal of Medical Genetics. Part A|September 24, 2017
The spectrum of DNMT3A variants in Tatton-Brown-Rahman syndrome overlaps with that in hematologic malignanciesWei Shen, Jennifer M Heeley, Colleen M Carlston, et al.
Nature Genetics|November 17, 2009
Exome sequencing identifies the cause of a mendelian disorderSarah B Ng, Kati J Buckingham, Choli Lee, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
American Journal of Medical Genetics. Part A|April 26, 2012
Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harmsHolly K Tabor, Jacquie Stock, Tracy Brazg, et al.
American Journal of Medical Genetics. Part A|April 24, 2013
Practices and policies of clinical exome sequencing providers: analysis and implicationsSeema M Jamal, Joon-Ho Yu, Jessica X Chong, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 3, 2004
Methodology of a multistate study of congenital hearing loss: preliminary data from Utah newborn screeningKarin M Dent, Aileen Kenneson, Janice C Palumbos, et al.
Journal of Genetic Counseling|May 7, 2025
Genetic counseling program director competencies as proposed by the program leadership development subcommittee of the Genetic Counselor Educators AssociationMonica L Marvin, Dawn C Allain, Erin P Carmany, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2016
My46: a Web-based tool for self-guided management of genomic test results in research and clinical settingsHolly K Tabor, Seema M Jamal, Joon-Ho Yu, et al.
American Journal of Medical Genetics. Part A|January 19, 2020
Novel KIAA1033/WASHC4 mutations in three patients with syndromic intellectual disability and a review of the literatureMirna Assoum, Ange-Line Bruel, Melissa L Crenshaw, et al.
American Journal of Medical Genetics. Part A|September 24, 2017
The spectrum of DNMT3A variants in Tatton-Brown-Rahman syndrome overlaps with that in hematologic malignanciesWei Shen, Jennifer M Heeley, Colleen M Carlston, et al.
Nature Genetics|November 17, 2009
Exome sequencing identifies the cause of a mendelian disorderSarah B Ng, Kati J Buckingham, Choli Lee, et al.
Pageof 2