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G Buchan

Showing results (81-90 of 96) with videos related to

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American Heart Journal|October 31, 2007
Preoperative neutrophil-lymphocyte ratio and outcome from coronary artery bypass graftingPatrick H Gibson, Bernard L Croal, Brian H Cuthbertson, et al.
The Journal of Molecular Diagnostics : JMD|January 25, 2022
A Framework of Critical Considerations in Clinical Exome Reanalyses by Clinical and Laboratory Standards InstituteMarco L Leung, Jianling Ji, Samuel Baker, et al.
British Journal of Anaesthesia|August 29, 2009
N-terminal pro-B-type natriuretic peptide levels and early outcome after cardiac surgery: a prospective cohort studyB H Cuthbertson, B L Croal, D Rae, et al.
Frontiers in Oncology|March 21, 2024
Looking beyond year 1 in the molecular era of pediatric brain tumor diagnosis: confirmatory testing of germline variants found on tumor sequencingBrittany L Greene, Shannon M Stasi, Michelle A Ting, et al.
Neurology|May 20, 2009
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophyM C Hannibal, E K Ruzzo, L R Miller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
Long-read genome sequencing identifies causal structural variation in a Mendelian diseaseJason D Merker, Aaron M Wenger, Tam Sneddon, et al.
NPJ Genomic Medicine|October 28, 2020
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline diseaseChristian R Marshall, Shimul Chowdhury, Ryan J Taft, et al.
Transfusion|September 17, 2025
Long-read DNA sequencing resolves a rare case of alloimmune hemolysis mimicking autoimmune hemolysisHui Xiao Chao, Thomas Ma, Livia Hegerova, et al.
Genetics in Medicine Open|October 18, 2024
3-hour genome sequencing and targeted analysis to rapidly assess genetic riskMiranda Pg Zalusky, Jonas A Gustafson, Stephanie C Bohaczuk, et al.
Human Molecular Genetics|May 17, 2014
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosisJillian G Buchan, David M Alvarado, Gabe E Haller, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
American Heart Journal|October 31, 2007
Preoperative neutrophil-lymphocyte ratio and outcome from coronary artery bypass graftingPatrick H Gibson, Bernard L Croal, Brian H Cuthbertson, et al.
The Journal of Molecular Diagnostics : JMD|January 25, 2022
A Framework of Critical Considerations in Clinical Exome Reanalyses by Clinical and Laboratory Standards InstituteMarco L Leung, Jianling Ji, Samuel Baker, et al.
British Journal of Anaesthesia|August 29, 2009
N-terminal pro-B-type natriuretic peptide levels and early outcome after cardiac surgery: a prospective cohort studyB H Cuthbertson, B L Croal, D Rae, et al.
Frontiers in Oncology|March 21, 2024
Looking beyond year 1 in the molecular era of pediatric brain tumor diagnosis: confirmatory testing of germline variants found on tumor sequencingBrittany L Greene, Shannon M Stasi, Michelle A Ting, et al.
Neurology|May 20, 2009
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophyM C Hannibal, E K Ruzzo, L R Miller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
Long-read genome sequencing identifies causal structural variation in a Mendelian diseaseJason D Merker, Aaron M Wenger, Tam Sneddon, et al.
NPJ Genomic Medicine|October 28, 2020
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline diseaseChristian R Marshall, Shimul Chowdhury, Ryan J Taft, et al.
Transfusion|September 17, 2025
Long-read DNA sequencing resolves a rare case of alloimmune hemolysis mimicking autoimmune hemolysisHui Xiao Chao, Thomas Ma, Livia Hegerova, et al.
Genetics in Medicine Open|October 18, 2024
3-hour genome sequencing and targeted analysis to rapidly assess genetic riskMiranda Pg Zalusky, Jonas A Gustafson, Stephanie C Bohaczuk, et al.
Human Molecular Genetics|May 17, 2014
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosisJillian G Buchan, David M Alvarado, Gabe E Haller, et al.
Pageof 10