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

Wayne W Grody

Showing results (41-50 of 133) with videos related to

Pageof 14
Sort By:
International Journal of Molecular Sciences|July 14, 2023
Synonymous Variants of Uncertain SilenceChristopher J Giacoletto, Jerome I Rotter, Wayne W Grody, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 6, 2021
Addendum: American College of Medical Genetics consensus statement on factor V Leiden mutation testingSucheta Bhatt, Annette K Taylor, Reymundo Lozano, et al.
American Journal of Ophthalmology|July 4, 2002
Discordant pursuit asymmetry and esotropia in monozygous twinsPradeep Sharma, Arthur L Rosenbaum, Terre Vives, et al.
Journal of Genetic Counseling|February 24, 2007
Sharing GJB2/GJB6 genetic test information with family membersTerri Blase, Ariadna Martinez, Wayne W Grody, et al.
Clinical Chemistry|June 1, 2010
Direct-to-consumer genotyping: are we ready for a brave new world?Lew Bender, Lawrence M Silverman, Mary Beth Dinulos, et al.
Molecular Oncology|March 31, 2015
Instability of a dinucleotide repeat in the 3'-untranslated region (UTR) of the microsomal prostaglandin E synthase-1 (mPGES-1) gene in microsatellite instability-high (MSI-H) colorectal carcinomaDurga Prasad Cherukuri, Joshua L Deignan, Kingshuk Das, et al.
American Journal of Medical Genetics. Part A|July 1, 2021
Central 22q11.2 deletion (LCR22 B-D) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndromeIsabella Lin, Yalda Afshar, Jeffrey Goldstein, et al.
Molecular Genetics and Metabolism|March 27, 2002
Cloning and characterization of human agmatinaseRamaswamy K Iyer, Ho K Kim, Rosemarie W Tsoa, et al.
Molecular Genetics and Metabolism|March 31, 2004
Arginases I and II: do their functions overlap?Stephen D Cederbaum, Hong Yu, Wayne W Grody, et al.
Archives of Otolaryngology--Head & Neck Surgery|November 23, 2005
Prelingual siblings of children with GJB2 hearing loss: issues to considerChristina G S Palmer, Ariadna Martinez, Yvonne Sininger, et al.
Pageof 14

Showing results (41-50 of 133) with videos related to

Sort By:
Pageof 14
International Journal of Molecular Sciences|July 14, 2023
Synonymous Variants of Uncertain SilenceChristopher J Giacoletto, Jerome I Rotter, Wayne W Grody, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 6, 2021
Addendum: American College of Medical Genetics consensus statement on factor V Leiden mutation testingSucheta Bhatt, Annette K Taylor, Reymundo Lozano, et al.
American Journal of Ophthalmology|July 4, 2002
Discordant pursuit asymmetry and esotropia in monozygous twinsPradeep Sharma, Arthur L Rosenbaum, Terre Vives, et al.
Journal of Genetic Counseling|February 24, 2007
Sharing GJB2/GJB6 genetic test information with family membersTerri Blase, Ariadna Martinez, Wayne W Grody, et al.
Clinical Chemistry|June 1, 2010
Direct-to-consumer genotyping: are we ready for a brave new world?Lew Bender, Lawrence M Silverman, Mary Beth Dinulos, et al.
Molecular Oncology|March 31, 2015
Instability of a dinucleotide repeat in the 3'-untranslated region (UTR) of the microsomal prostaglandin E synthase-1 (mPGES-1) gene in microsatellite instability-high (MSI-H) colorectal carcinomaDurga Prasad Cherukuri, Joshua L Deignan, Kingshuk Das, et al.
American Journal of Medical Genetics. Part A|July 1, 2021
Central 22q11.2 deletion (LCR22 B-D) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndromeIsabella Lin, Yalda Afshar, Jeffrey Goldstein, et al.
Molecular Genetics and Metabolism|March 27, 2002
Cloning and characterization of human agmatinaseRamaswamy K Iyer, Ho K Kim, Rosemarie W Tsoa, et al.
Molecular Genetics and Metabolism|March 31, 2004
Arginases I and II: do their functions overlap?Stephen D Cederbaum, Hong Yu, Wayne W Grody, et al.
Archives of Otolaryngology--Head & Neck Surgery|November 23, 2005
Prelingual siblings of children with GJB2 hearing loss: issues to considerChristina G S Palmer, Ariadna Martinez, Yvonne Sininger, et al.
Pageof 14