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Wayne W Grody

Showing results (91-100 of 133) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2023
Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG)Joshua L Deignan, Anthony R Gregg, Wayne W Grody, et al.
Journal of Deaf Studies and Deaf Education|May 22, 2010
Deaf adults' reasons for genetic testing depend on cultural affiliation: results from a prospective, longitudinal genetic counseling and testing studyPatrick Boudreault, Erin E Baldwin, Michelle Fox, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2008
Infant hearing loss and connexin testing in a diverse populationLisa A Schimmenti, Ariadna Martinez, Milhan Telatar, et al.
Archives of Pathology & Laboratory Medicine|August 23, 2023
A Primer on Gene Editing: What Does It Mean for Pathologists?Allison Cushman-Vokoun, Ryan J Schmidt, Matthew Charles Hiemenz, et al.
Archives of Pathology & Laboratory Medicine|August 21, 2023
A Primer on Gene EditingAllison Cushman-Vokoun, Ryan J Schmidt, Matthew Charles Hiemenz, et al.
Archives of Pathology & Laboratory Medicine|December 12, 2025
A Primer on Gene Editing: What Does It Mean for Pathologists?Allison Cushman-Vokoun, Ryan J Schmidt, Matthew Charles Hiemenz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2002
Standards and guidelines for CFTR mutation testingCarolyn Sue Richards, Linda A Bradley, Jean Amos, et al.
BMC Medical Genetics|June 3, 2014
De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencingSamuel P Strom, Reymundo Lozano, Hane Lee, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 16, 2009
Short-term correction of arginase deficiency in a neonatal murine model with a helper-dependent adenoviral vectorChia-Ling Gau, Robin A Rosenblatt, Vincenzo Cerullo, et al.
Molecular Genetics and Metabolism|August 8, 2013
Lethal phenotype in conditional late-onset arginase 1 deficiency in the mouseJennifer Kasten, Chuhong Hu, Ragini Bhargava, et al.
Pageof 14

Showing results (91-100 of 133) with videos related to

Sort By:
Pageof 14
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2023
Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG)Joshua L Deignan, Anthony R Gregg, Wayne W Grody, et al.
Journal of Deaf Studies and Deaf Education|May 22, 2010
Deaf adults' reasons for genetic testing depend on cultural affiliation: results from a prospective, longitudinal genetic counseling and testing studyPatrick Boudreault, Erin E Baldwin, Michelle Fox, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2008
Infant hearing loss and connexin testing in a diverse populationLisa A Schimmenti, Ariadna Martinez, Milhan Telatar, et al.
Archives of Pathology & Laboratory Medicine|August 23, 2023
A Primer on Gene Editing: What Does It Mean for Pathologists?Allison Cushman-Vokoun, Ryan J Schmidt, Matthew Charles Hiemenz, et al.
Archives of Pathology & Laboratory Medicine|August 21, 2023
A Primer on Gene EditingAllison Cushman-Vokoun, Ryan J Schmidt, Matthew Charles Hiemenz, et al.
Archives of Pathology & Laboratory Medicine|December 12, 2025
A Primer on Gene Editing: What Does It Mean for Pathologists?Allison Cushman-Vokoun, Ryan J Schmidt, Matthew Charles Hiemenz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2002
Standards and guidelines for CFTR mutation testingCarolyn Sue Richards, Linda A Bradley, Jean Amos, et al.
BMC Medical Genetics|June 3, 2014
De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencingSamuel P Strom, Reymundo Lozano, Hane Lee, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 16, 2009
Short-term correction of arginase deficiency in a neonatal murine model with a helper-dependent adenoviral vectorChia-Ling Gau, Robin A Rosenblatt, Vincenzo Cerullo, et al.
Molecular Genetics and Metabolism|August 8, 2013
Lethal phenotype in conditional late-onset arginase 1 deficiency in the mouseJennifer Kasten, Chuhong Hu, Ragini Bhargava, et al.
Pageof 14