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Translational Pediatrics
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March 11, 2026
Diagnostic yield of exome and genome sequencing for critically ill pediatric cardiac patients
Angela C Onorato, Rachel Gosselin, Bimal P Chaudhari, et al.
Neoreviews
|
November 30, 2023
An Infant with Thickened and Hyperechoic Main Pulmonary Artery
Veronica Armstrong, Carl H Backes, Brian K Rivera, et al.
Human Mutation
|
April 14, 2025
CAVaLRi: An Algorithm for Rapid Identification of Diagnostic Germline Variation
Robert J Schuetz, Austin A Antoniou, Grant E Lammi, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
April 1, 2026
Bibliometric analysis of reviews of outcomes for adults with a complex perinatal history
Laura C Hart, Amrik Singh Khalsa, Austin A Antoniou, et al.
Neoreviews
|
March 1, 2024
Ethical and Legal Issues Surrounding Genetic Testing in the NICU
Katharine P Callahan, Ellen W Clayton, Amy A Lemke, et al.
Circulation. Genomic and Precision Medicine
|
February 10, 2026
Assessing Genetic Testing in Adult Congenital Heart Disease: Current State and Patient Perspectives
Angela Onorato, Kara Klinkebiel, Rachel Levenseller, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 25, 2026
PheBee: A Graph-Aware System for Scalable, Traceable, and Semantic Phenotyping
David M Gordon, Max Homilius, Austin A Antoniou, et al.
Cold Spring Harbor Molecular Case Studies
|
May 25, 2023
Perinatal-lethal nonimmune fetal hydrops attributed to <i>MECOM</i>-associated bone marrow failure
Camille A Dash, Jill A Madden, Christy Cummings, et al.
Pediatric Cardiology
|
November 20, 2025
Genetic Evaluation Practices for Neonates with Congenital Heart Disease in Pediatric Cardiac Intensive Care Units: Findings from a Multi-institutional Survey
Amee M Bigelow, Catherine D Krawczeski, Isaac Kistler, et al.
Cold Spring Harbor Molecular Case Studies
|
June 14, 2020
Early-onset Wilson disease caused by <i>ATP7B</i> exon skipping associated with intronic variant
Daniel C Koboldt, Scott E Hickey, Bimal P Chaudhari, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 49) with videos related to
Sort By:
Page
of 5
Translational Pediatrics
|
March 11, 2026
Diagnostic yield of exome and genome sequencing for critically ill pediatric cardiac patients
Angela C Onorato, Rachel Gosselin, Bimal P Chaudhari, et al.
Neoreviews
|
November 30, 2023
An Infant with Thickened and Hyperechoic Main Pulmonary Artery
Veronica Armstrong, Carl H Backes, Brian K Rivera, et al.
Human Mutation
|
April 14, 2025
CAVaLRi: An Algorithm for Rapid Identification of Diagnostic Germline Variation
Robert J Schuetz, Austin A Antoniou, Grant E Lammi, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
April 1, 2026
Bibliometric analysis of reviews of outcomes for adults with a complex perinatal history
Laura C Hart, Amrik Singh Khalsa, Austin A Antoniou, et al.
Neoreviews
|
March 1, 2024
Ethical and Legal Issues Surrounding Genetic Testing in the NICU
Katharine P Callahan, Ellen W Clayton, Amy A Lemke, et al.
Circulation. Genomic and Precision Medicine
|
February 10, 2026
Assessing Genetic Testing in Adult Congenital Heart Disease: Current State and Patient Perspectives
Angela Onorato, Kara Klinkebiel, Rachel Levenseller, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 25, 2026
PheBee: A Graph-Aware System for Scalable, Traceable, and Semantic Phenotyping
David M Gordon, Max Homilius, Austin A Antoniou, et al.
Cold Spring Harbor Molecular Case Studies
|
May 25, 2023
Perinatal-lethal nonimmune fetal hydrops attributed to <i>MECOM</i>-associated bone marrow failure
Camille A Dash, Jill A Madden, Christy Cummings, et al.
Pediatric Cardiology
|
November 20, 2025
Genetic Evaluation Practices for Neonates with Congenital Heart Disease in Pediatric Cardiac Intensive Care Units: Findings from a Multi-institutional Survey
Amee M Bigelow, Catherine D Krawczeski, Isaac Kistler, et al.
Cold Spring Harbor Molecular Case Studies
|
June 14, 2020
Early-onset Wilson disease caused by <i>ATP7B</i> exon skipping associated with intronic variant
Daniel C Koboldt, Scott E Hickey, Bimal P Chaudhari, et al.
Page
of 5