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Richard Redon

Showing results (21-30 of 131) with videos related to

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Frontiers in Cardiovascular Medicine|May 21, 2016
The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex InheritanceJean-Baptiste Gourraud, Julien Barc, Aurélie Thollet, et al.
Cells|December 11, 2022
Deciphering Transcriptional Networks during Human Cardiac DevelopmentRobin Canac, Bastien Cimarosti, Aurore Girardeau, et al.
European Journal of Human Genetics : EJHG|March 30, 2006
Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndromeRichard Redon, Geneviève Baujat, Damien Sanlaville, et al.
G3 (Bethesda, Md.)|December 10, 2024
SURFBAT: a surrogate family based association test building on large imputation reference panelsAnthony F Herzig, Simone Rubinacci, Gaëlle Marenne, et al.
Cancer Research|September 18, 2004
Genomic and expression profiling of chromosome 17 in breast cancer reveals complex patterns of alterations and novel candidate genesBéatrice Orsetti, Mélanie Nugoli, Nathalie Cervera, et al.
Journal of the American College of Cardiology|March 25, 2017
Familial Catecholamine-Induced QT Prolongation in Unexplained Sudden Cardiac DeathFrancois Huchet, Florence Kyndt, Julien Barc, et al.
Stem Cell Research|January 7, 2022
Generation of human induced pluripotent stem cell lines from two patients affected by catecholamine-induced QT prolongation (CIQTP)Bastien Cimarosti, Robin Canac, Aurore Girardeau, et al.
American Journal of Human Genetics|April 17, 2007
Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunctionJeanne Amiel, Marlene Rio, Loic de Pontual, et al.
BMC Genomics|June 15, 2013
Large scale variation in DNA copy number in chicken breedsRichard P M A Crooijmans, Mark S Fife, Tomas W Fitzgerald, et al.
Plos One|July 26, 2017
DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with diseaseElodie Persyn, Matilde Karakachoff, Solena Le Scouarnec, et al.
Pageof 14

Showing results (21-30 of 131) with videos related to

Sort By:
Pageof 14
Frontiers in Cardiovascular Medicine|May 21, 2016
The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex InheritanceJean-Baptiste Gourraud, Julien Barc, Aurélie Thollet, et al.
Cells|December 11, 2022
Deciphering Transcriptional Networks during Human Cardiac DevelopmentRobin Canac, Bastien Cimarosti, Aurore Girardeau, et al.
European Journal of Human Genetics : EJHG|March 30, 2006
Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndromeRichard Redon, Geneviève Baujat, Damien Sanlaville, et al.
G3 (Bethesda, Md.)|December 10, 2024
SURFBAT: a surrogate family based association test building on large imputation reference panelsAnthony F Herzig, Simone Rubinacci, Gaëlle Marenne, et al.
Cancer Research|September 18, 2004
Genomic and expression profiling of chromosome 17 in breast cancer reveals complex patterns of alterations and novel candidate genesBéatrice Orsetti, Mélanie Nugoli, Nathalie Cervera, et al.
Journal of the American College of Cardiology|March 25, 2017
Familial Catecholamine-Induced QT Prolongation in Unexplained Sudden Cardiac DeathFrancois Huchet, Florence Kyndt, Julien Barc, et al.
Stem Cell Research|January 7, 2022
Generation of human induced pluripotent stem cell lines from two patients affected by catecholamine-induced QT prolongation (CIQTP)Bastien Cimarosti, Robin Canac, Aurore Girardeau, et al.
American Journal of Human Genetics|April 17, 2007
Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunctionJeanne Amiel, Marlene Rio, Loic de Pontual, et al.
BMC Genomics|June 15, 2013
Large scale variation in DNA copy number in chicken breedsRichard P M A Crooijmans, Mark S Fife, Tomas W Fitzgerald, et al.
Plos One|July 26, 2017
DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with diseaseElodie Persyn, Matilde Karakachoff, Solena Le Scouarnec, et al.
Pageof 14