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Showing results (91-100 of 96) with videos related to

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Human Biology|May 1, 1999
Cystic fibrosis: low frequency of DF508 mutation in 2 population samples from Rio de Janeiro, BrazilG M Cabello, A F Moreira, D Horovitz, et al.
Journal of Genetic Counseling|August 27, 2024
Expanded carrier screening for inherited genetic disease using exome and genome sequencingN Belnap, K Ramsey, A Abraham, et al.
Gene Therapy|February 8, 2013
AAV-based gene therapy prevents neuropathology and results in normal cognitive development in the hyperargininemic mouseE K Lee, C Hu, R Bhargava, et al.
Clinical Genetics|October 9, 2012
The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLAF S Ong, H Vakil, Y Xue, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 22, 2024
ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individualsE De Wachter, K De Boeck, I Sermet-Gaudelus, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001
Issues in implementing prenatal screening for cystic fibrosis: results of a working conferenceJ E Haddow, L A Bradley, G E Palomaki, et al.
Pageof 10

Showing results (91-100 of 96) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 96 results.
Human Biology|May 1, 1999
Cystic fibrosis: low frequency of DF508 mutation in 2 population samples from Rio de Janeiro, BrazilG M Cabello, A F Moreira, D Horovitz, et al.
Journal of Genetic Counseling|August 27, 2024
Expanded carrier screening for inherited genetic disease using exome and genome sequencingN Belnap, K Ramsey, A Abraham, et al.
Gene Therapy|February 8, 2013
AAV-based gene therapy prevents neuropathology and results in normal cognitive development in the hyperargininemic mouseE K Lee, C Hu, R Bhargava, et al.
Clinical Genetics|October 9, 2012
The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLAF S Ong, H Vakil, Y Xue, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 22, 2024
ECFS standards of care on CFTR-related disorders: Towards a comprehensive program for affected individualsE De Wachter, K De Boeck, I Sermet-Gaudelus, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001
Issues in implementing prenatal screening for cystic fibrosis: results of a working conferenceJ E Haddow, L A Bradley, G E Palomaki, et al.
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