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Ronald D Cohn

Showing results (21-30 of 100) with videos related to

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Frontiers in Molecular Neuroscience|December 6, 2021
Editorial: Current Insights Into LAMA2 DiseaseStefano C Previtali, Ronald D Cohn, Markus A Ruegg
JAMA|January 31, 2008
The genetics revolution and primary care pediatricsTina L Cheng, Ronald D Cohn, George J Dover
Seizure|March 30, 2019
MEF2C-related epilepsy: Delineating the phenotypic spectrum from a novel mutation and literature reviewFelippe Borlot, Robyn Whitney, Ronald D Cohn, et al.
Human Mutation|March 7, 2014
The genome clinic: a multidisciplinary approach to assessing the opportunities and challenges of integrating genomic analysis into clinical careSarah Bowdin, Peter N Ray, Ronald D Cohn, et al.
Nature Biotechnology|January 29, 2024
An optimized toolkit for prime editingRyan M Marks, Ori Scott, Evgueni A Ivakine, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|October 26, 2021
Genome sequencing as a diagnostic testGregory Costain, Ronald D Cohn, Stephen W Scherer, et al.
American Journal of Medical Genetics. Part A|September 11, 2017
Treating pediatric neuromuscular disorders: The future is nowJames J Dowling, Hernan D Gonorazky, Ronald D Cohn, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 16, 2018
Outcome of Patients With Inherited Neurotransmitter DisordersDawn Cordeiro, Garrett Bullivant, Ronald D Cohn, et al.
Children (Basel, Switzerland)|May 23, 2017
Genetic Testing among Children in a Complex Care ProgramKrista Oei, Robin Z Hayeems, Wendy J Ungar, et al.
Molecular Genetics & Genomic Medicine|April 11, 2018
ERCC6L2-associated inherited bone marrow failure syndromeIren Shabanova, Elisa Cohen, Michaela Cada, et al.
Pageof 10

Showing results (21-30 of 100) with videos related to

Sort By:
Pageof 10
Frontiers in Molecular Neuroscience|December 6, 2021
Editorial: Current Insights Into LAMA2 DiseaseStefano C Previtali, Ronald D Cohn, Markus A Ruegg
JAMA|January 31, 2008
The genetics revolution and primary care pediatricsTina L Cheng, Ronald D Cohn, George J Dover
Seizure|March 30, 2019
MEF2C-related epilepsy: Delineating the phenotypic spectrum from a novel mutation and literature reviewFelippe Borlot, Robyn Whitney, Ronald D Cohn, et al.
Human Mutation|March 7, 2014
The genome clinic: a multidisciplinary approach to assessing the opportunities and challenges of integrating genomic analysis into clinical careSarah Bowdin, Peter N Ray, Ronald D Cohn, et al.
Nature Biotechnology|January 29, 2024
An optimized toolkit for prime editingRyan M Marks, Ori Scott, Evgueni A Ivakine, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|October 26, 2021
Genome sequencing as a diagnostic testGregory Costain, Ronald D Cohn, Stephen W Scherer, et al.
American Journal of Medical Genetics. Part A|September 11, 2017
Treating pediatric neuromuscular disorders: The future is nowJames J Dowling, Hernan D Gonorazky, Ronald D Cohn, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 16, 2018
Outcome of Patients With Inherited Neurotransmitter DisordersDawn Cordeiro, Garrett Bullivant, Ronald D Cohn, et al.
Children (Basel, Switzerland)|May 23, 2017
Genetic Testing among Children in a Complex Care ProgramKrista Oei, Robin Z Hayeems, Wendy J Ungar, et al.
Molecular Genetics & Genomic Medicine|April 11, 2018
ERCC6L2-associated inherited bone marrow failure syndromeIren Shabanova, Elisa Cohen, Michaela Cada, et al.
Pageof 10