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Alejandro Blanco-Verea

Showing results (11-20 of 27) with videos related to

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European Journal of Clinical Investigation|July 22, 2016
PRKG1 and genetic diagnosis of early-onset thoracic aortic diseaseMarina Gago-Díaz, Alejandro Blanco-Verea, Gisela Teixidó, et al.
Forensic Science International|February 25, 2012
Sarcomeric gene mutations in sudden infant death syndrome (SIDS)Maria Brion, Catarina Allegue, Montserrat Santori, et al.
Annals of Clinical and Laboratory Science|August 7, 2010
Identification of a novel MYBPC3 gene variant in a patient with hypertrophic cardiomyopathyMaria Brion, Catarina Allegue, Rocio Gil, et al.
Forensic Science International|November 12, 2018
Sudden unexpected death in the young - Value of massive parallel sequencing in postmortem genetic analysesStefanie Scheiper, Eva Ramos-Luis, Alejandro Blanco-Verea, et al.
Heart (British Cardiac Society)|November 1, 2024
Prevalence and relevance of H558R in the efficacy and toxicity of flecainide in patients with atrial fibrillation: a cohort studyMauro Trincado Ave, Maria Brion, Alejandro Blanco-Verea, et al.
Forensic Science International. Genetics|September 16, 2019
Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillationMontserrat Santori, Rocío Gil, Alejandro Blanco-Verea, et al.
Plos One|August 12, 2009
Ancestry analysis in the 11-M Madrid bomb attack investigationChristopher Phillips, Lourdes Prieto, Manuel Fondevila, et al.
International Journal of Legal Medicine|April 10, 2017
Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissectionMarina Gago-Díaz, Eva Ramos-Luis, Silvia Zoppis, et al.
Molecular Diagnosis & Therapy|December 1, 2022
Detection of the Copy Number Variants of Genes in Patients with Familial Cardiac Diseases by Massively Parallel SequencingAlejandro Blanco-Verea, Brais Piñeiro, Rocio Gil, et al.
Electrophoresis|November 8, 2005
Introduction of an single nucleodite polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineagesMaría Brión, Juan J Sanchez, Kinga Balogh, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
European Journal of Clinical Investigation|July 22, 2016
PRKG1 and genetic diagnosis of early-onset thoracic aortic diseaseMarina Gago-Díaz, Alejandro Blanco-Verea, Gisela Teixidó, et al.
Forensic Science International|February 25, 2012
Sarcomeric gene mutations in sudden infant death syndrome (SIDS)Maria Brion, Catarina Allegue, Montserrat Santori, et al.
Annals of Clinical and Laboratory Science|August 7, 2010
Identification of a novel MYBPC3 gene variant in a patient with hypertrophic cardiomyopathyMaria Brion, Catarina Allegue, Rocio Gil, et al.
Forensic Science International|November 12, 2018
Sudden unexpected death in the young - Value of massive parallel sequencing in postmortem genetic analysesStefanie Scheiper, Eva Ramos-Luis, Alejandro Blanco-Verea, et al.
Heart (British Cardiac Society)|November 1, 2024
Prevalence and relevance of H558R in the efficacy and toxicity of flecainide in patients with atrial fibrillation: a cohort studyMauro Trincado Ave, Maria Brion, Alejandro Blanco-Verea, et al.
Forensic Science International. Genetics|September 16, 2019
Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillationMontserrat Santori, Rocío Gil, Alejandro Blanco-Verea, et al.
Plos One|August 12, 2009
Ancestry analysis in the 11-M Madrid bomb attack investigationChristopher Phillips, Lourdes Prieto, Manuel Fondevila, et al.
International Journal of Legal Medicine|April 10, 2017
Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissectionMarina Gago-Díaz, Eva Ramos-Luis, Silvia Zoppis, et al.
Molecular Diagnosis & Therapy|December 1, 2022
Detection of the Copy Number Variants of Genes in Patients with Familial Cardiac Diseases by Massively Parallel SequencingAlejandro Blanco-Verea, Brais Piñeiro, Rocio Gil, et al.
Electrophoresis|November 8, 2005
Introduction of an single nucleodite polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineagesMaría Brión, Juan J Sanchez, Kinga Balogh, et al.
Pageof 3