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Candice Silversides

Showing results (61-70 of 64) with videos related to

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The Canadian Journal of Cardiology|April 23, 2022
Canadian Cardiovascular Society 2022 Guidelines for Cardiovascular Interventions in Adults With Congenital Heart DiseaseAriane Marelli, Luc Beauchesne, Jack Colman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndromeErik Boot, Sólveig Óskarsdóttir, Joanne C Y Loo, et al.
Journal of Cardiovascular Development and Disease|September 27, 2023
Design and Harmonization Approach for the Multi-Institutional Neurocognitive Discovery Study (MINDS) of Adult Congenital Heart Disease (ACHD) Neuroimaging Ancillary Study: A Technical NoteAshok Panigrahy, Vanessa Schmithorst, Rafael Ceschin, et al.
American Journal of Human Genetics|March 5, 2013
Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromesMaria Delio, Tingwei Guo, Donna M McDonald-McGinn, et al.
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Showing results (61-70 of 64) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 64 results.
The Canadian Journal of Cardiology|April 23, 2022
Canadian Cardiovascular Society 2022 Guidelines for Cardiovascular Interventions in Adults With Congenital Heart DiseaseAriane Marelli, Luc Beauchesne, Jack Colman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndromeErik Boot, Sólveig Óskarsdóttir, Joanne C Y Loo, et al.
Journal of Cardiovascular Development and Disease|September 27, 2023
Design and Harmonization Approach for the Multi-Institutional Neurocognitive Discovery Study (MINDS) of Adult Congenital Heart Disease (ACHD) Neuroimaging Ancillary Study: A Technical NoteAshok Panigrahy, Vanessa Schmithorst, Rafael Ceschin, et al.
American Journal of Human Genetics|March 5, 2013
Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromesMaria Delio, Tingwei Guo, Donna M McDonald-McGinn, et al.
Pageof 7