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

Jan M Friedman

Showing results (91-100 of 165) with videos related to

Pageof 17
Sort By:
European Journal of Medical Genetics|September 24, 2009
A characteristic syndrome associated with microduplication of 8q12, inclusive of CHD7Anna M Lehman, Jan M Friedman, David Chai, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 28, 2004
Communicating risks during pregnancy: a workshop on the use of data from animal developmental toxicity studies in pregnancy labels for drugsAnthony R Scialli, Judy L Buelke-Sam, Christina D Chambers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 14, 2018
Genome-wide sequencing in acutely ill infants: genomic medicine's critical application?Jan M Friedman, Yvonne Bombard, Martina C Cornel, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Quantitative associations of scalp and body subcutaneous neurofibromas with internal plexiform tumors in neurofibromatosis 1Kimberly Jett, Rosa Nguyen, Darian Arman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 12, 2020
Correction: The composition and capacity of the clinical genetics workforce in high-income countries: a scoping reviewNick Dragojlovic, Kennedy Borle, Nicola Kopac, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 25, 2020
The composition and capacity of the clinical genetics workforce in high-income countries: a scoping reviewNick Dragojlovic, Kennedy Borle, Nicola Kopac, et al.
Genome Medicine|September 14, 2021
Correction to: Genome-wide sequencing as a first-tier screening test for short tandem repeat expansionsIndhu-Shree Rajan-Babu, Junran J Peng, Readman Chiu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 24, 2022
COVID-19 in people with neurofibromatosis 1, neurofibromatosis 2, or schwannomatosisJineta Banerjee, Jan M Friedman, Laura J Klesse, et al.
Journal of Medical Genetics|July 10, 2025
Commentary on <i>UBTF</i> haploinsufficiency associated with <i>UBTF</i>-related global developmental delay and distinctive facial features without neuroregressionTony Yammine, Sandra Mercier, Céline Poirsier, et al.
Genome Medicine|August 10, 2021
Genome-wide sequencing as a first-tier screening test for short tandem repeat expansionsIndhu-Shree Rajan-Babu, Junran J Peng, Readman Chiu, et al.
Pageof 17

Showing results (91-100 of 165) with videos related to

Sort By:
Pageof 17
European Journal of Medical Genetics|September 24, 2009
A characteristic syndrome associated with microduplication of 8q12, inclusive of CHD7Anna M Lehman, Jan M Friedman, David Chai, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 28, 2004
Communicating risks during pregnancy: a workshop on the use of data from animal developmental toxicity studies in pregnancy labels for drugsAnthony R Scialli, Judy L Buelke-Sam, Christina D Chambers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 14, 2018
Genome-wide sequencing in acutely ill infants: genomic medicine's critical application?Jan M Friedman, Yvonne Bombard, Martina C Cornel, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Quantitative associations of scalp and body subcutaneous neurofibromas with internal plexiform tumors in neurofibromatosis 1Kimberly Jett, Rosa Nguyen, Darian Arman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 12, 2020
Correction: The composition and capacity of the clinical genetics workforce in high-income countries: a scoping reviewNick Dragojlovic, Kennedy Borle, Nicola Kopac, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 25, 2020
The composition and capacity of the clinical genetics workforce in high-income countries: a scoping reviewNick Dragojlovic, Kennedy Borle, Nicola Kopac, et al.
Genome Medicine|September 14, 2021
Correction to: Genome-wide sequencing as a first-tier screening test for short tandem repeat expansionsIndhu-Shree Rajan-Babu, Junran J Peng, Readman Chiu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 24, 2022
COVID-19 in people with neurofibromatosis 1, neurofibromatosis 2, or schwannomatosisJineta Banerjee, Jan M Friedman, Laura J Klesse, et al.
Journal of Medical Genetics|July 10, 2025
Commentary on <i>UBTF</i> haploinsufficiency associated with <i>UBTF</i>-related global developmental delay and distinctive facial features without neuroregressionTony Yammine, Sandra Mercier, Céline Poirsier, et al.
Genome Medicine|August 10, 2021
Genome-wide sequencing as a first-tier screening test for short tandem repeat expansionsIndhu-Shree Rajan-Babu, Junran J Peng, Readman Chiu, et al.
Pageof 17