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American Journal of Medical Genetics. Part A
|
October 21, 2009
Characterization of a new X-linked mental retardation syndrome with microcephaly, cortical malformation, and thin habitus
Christèle du Souich, Athena Chou, Jingyi Yin, et al.
The Canadian Journal of Cardiology
|
June 16, 2024
Canadian Cardiovascular Society Clinical Practice Update on Contemporary Management of the Patient With Hypertrophic Cardiomyopathy
Andrew M Crean, Arnon Adler, Laura Arbour, et al.
Lancet Regional Health. Americas
|
April 2, 2025
Hospital admissions for acute respiratory tract infections among infants from Nunavut and the burden of respiratory syncytial virus: a 10-year retrospective cohort study
Mai-Lei Woo Kinshella, Jean Allen, Jasmine Pawa, et al.
American Journal of Human Genetics
|
September 6, 2002
The gene for juvenile hyaline fibromatosis maps to chromosome 4q21
Nazneen Rahman, Melanie Dunstan, M Dawn Teare, et al.
Circulation. Cardiovascular Genetics
|
June 11, 2017
Genetic Testing in the Evaluation of Unexplained Cardiac Arrest: From the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry)
Greg Mellor, Zachary W M Laksman, Rafik Tadros, et al.
American Journal of Human Genetics
|
September 26, 2003
Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis
Sandra Hanks, Sarah Adams, Jenny Douglas, et al.
Circulation. Genomic and Precision Medicine
|
May 7, 2021
Variant Reinterpretation in Survivors of Cardiac Arrest With Preserved Ejection Fraction (the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry) by Clinicians and Clinical Commercial Laboratories
Brianna Davies, Kirsten Bartels, Julie Hathaway, et al.
Circulation. Genomic and Precision Medicine
|
July 29, 2024
High-Risk Nonclassical Long-QT Syndrome Genotypes: Spectrum of Genetic and Phenotypic Features
Abdulkarim Abdulrahman, Brianna Davies, Habib Khan, et al.
JACC. Clinical Electrophysiology
|
November 24, 2018
Early Repolarization Pattern Inheritance in the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry (CASPER)
Navraj Malhi, Petsy P So, Christopher C Cheung, et al.
Frontiers in Pediatrics
|
December 31, 2020
Barriers and Considerations for Diagnosing Rare Diseases in Indigenous Populations
Carla S D'Angelo, Azure Hermes, Christopher R McMaster, et al.
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Search research articles
Search
Showing results (91-100 of 118) with videos related to
Sort By:
Page
of 12
American Journal of Medical Genetics. Part A
|
October 21, 2009
Characterization of a new X-linked mental retardation syndrome with microcephaly, cortical malformation, and thin habitus
Christèle du Souich, Athena Chou, Jingyi Yin, et al.
The Canadian Journal of Cardiology
|
June 16, 2024
Canadian Cardiovascular Society Clinical Practice Update on Contemporary Management of the Patient With Hypertrophic Cardiomyopathy
Andrew M Crean, Arnon Adler, Laura Arbour, et al.
Lancet Regional Health. Americas
|
April 2, 2025
Hospital admissions for acute respiratory tract infections among infants from Nunavut and the burden of respiratory syncytial virus: a 10-year retrospective cohort study
Mai-Lei Woo Kinshella, Jean Allen, Jasmine Pawa, et al.
American Journal of Human Genetics
|
September 6, 2002
The gene for juvenile hyaline fibromatosis maps to chromosome 4q21
Nazneen Rahman, Melanie Dunstan, M Dawn Teare, et al.
Circulation. Cardiovascular Genetics
|
June 11, 2017
Genetic Testing in the Evaluation of Unexplained Cardiac Arrest: From the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry)
Greg Mellor, Zachary W M Laksman, Rafik Tadros, et al.
American Journal of Human Genetics
|
September 26, 2003
Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis
Sandra Hanks, Sarah Adams, Jenny Douglas, et al.
Circulation. Genomic and Precision Medicine
|
May 7, 2021
Variant Reinterpretation in Survivors of Cardiac Arrest With Preserved Ejection Fraction (the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry) by Clinicians and Clinical Commercial Laboratories
Brianna Davies, Kirsten Bartels, Julie Hathaway, et al.
Circulation. Genomic and Precision Medicine
|
July 29, 2024
High-Risk Nonclassical Long-QT Syndrome Genotypes: Spectrum of Genetic and Phenotypic Features
Abdulkarim Abdulrahman, Brianna Davies, Habib Khan, et al.
JACC. Clinical Electrophysiology
|
November 24, 2018
Early Repolarization Pattern Inheritance in the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry (CASPER)
Navraj Malhi, Petsy P So, Christopher C Cheung, et al.
Frontiers in Pediatrics
|
December 31, 2020
Barriers and Considerations for Diagnosing Rare Diseases in Indigenous Populations
Carla S D'Angelo, Azure Hermes, Christopher R McMaster, et al.
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of 12