Search research articles
Contact Us
Filters
Showing results (11-20 of 27) with videos related to
Page
of 3
Sort By:
European Journal of Clinical Investigation
|
July 22, 2016
PRKG1 and genetic diagnosis of early-onset thoracic aortic disease
Marina 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 cardiomyopathy
Maria 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 analyses
Stefanie 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 study
Mauro 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 fibrillation
Montserrat Santori, Rocío Gil, Alejandro Blanco-Verea, et al.
Plos One
|
August 12, 2009
Ancestry analysis in the 11-M Madrid bomb attack investigation
Christopher 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 dissection
Marina 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 Sequencing
Alejandro 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 lineages
María Brión, Juan J Sanchez, Kinga Balogh, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
European Journal of Clinical Investigation
|
July 22, 2016
PRKG1 and genetic diagnosis of early-onset thoracic aortic disease
Marina 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 cardiomyopathy
Maria 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 analyses
Stefanie 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 study
Mauro 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 fibrillation
Montserrat Santori, Rocío Gil, Alejandro Blanco-Verea, et al.
Plos One
|
August 12, 2009
Ancestry analysis in the 11-M Madrid bomb attack investigation
Christopher 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 dissection
Marina 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 Sequencing
Alejandro 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 lineages
María Brión, Juan J Sanchez, Kinga Balogh, et al.
Page
of 3