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Pedro Arias

Showing results (31-40 of 84) with videos related to

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Diabetes Research and Clinical Practice|May 5, 2009
Identification of eight new mutations in the GCK gene by DHPLC screening in a Spanish populationJesús Solera, Pedro Arias, Cintia Amiñoso, et al.
Pharmacogenetics and Genomics|June 11, 2021
Analytical validation of a laboratory-development multigene pharmacogenetic assayRocío Rosas-Alonso, Javier Queiruga, Pedro Arias, et al.
Cells|November 27, 2021
Expanding the Evidence of a Semi-Dominant Inheritance in <i>GDF2</i> Associated with Pulmonary Arterial HypertensionNatalia Gallego, Alejandro Cruz-Utrilla, Inmaculada Guillén, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 10, 2023
Adult experiences in Beckwith-Wiedemann syndromeWilliam A Drust, Alessandro Mussa, Andrea Gazzin, et al.
Genes|May 28, 2022
Description of Two New Cases of <i>AQP1</i> Related Pulmonary Arterial Hypertension and Review of the LiteratureNatalia Gallego-Zazo, Alejandro Cruz-Utrilla, María Jesús Del Cerro, et al.
Clinical Genetics|October 31, 2023
Genetic and phenotypic findings in 34 novel Spanish patients with DDX3X neurodevelopmental disorderAlejandro Parra, Patricia Pascual, Mario Cazalla, et al.
Revista Espanola De Cardiologia (English Ed.)|July 26, 2016
Molecular Analysis of BMPR2, TBX4, and KCNK3 and Genotype-Phenotype Correlations in Spanish Patients and Families With Idiopathic and Hereditary Pulmonary Arterial HypertensionPaula Navas, Jair Tenorio, Carlos Andrés Quezada, et al.
Clinical Genetics|September 13, 2023
Lamb-Shaffer syndrome: 20 Spanish patients and literature review expands the view of neurodevelopmental disorders caused by SOX5 haploinsufficiencyJair Tenorio-Castano, Ángela Sánchez-Algaba Gómez, Mónica Coronado, et al.
Clinical Genetics|January 11, 2019
MRX93 syndrome (BRWD3 gene): five new patients with novel mutationsJair Tenorio, Pablo Alarcón, Pedro Arias, et al.
Clinical and Translational Science|December 2, 2017
Clinical Implementation of Pharmacogenetic Testing in a Hospital of the Spanish National Health System: Strategy and Experience Over 3 YearsAlberto M Borobia, Irene Dapia, Hoi Y Tong, et al.
Pageof 9

Showing results (31-40 of 84) with videos related to

Sort By:
Pageof 9
Diabetes Research and Clinical Practice|May 5, 2009
Identification of eight new mutations in the GCK gene by DHPLC screening in a Spanish populationJesús Solera, Pedro Arias, Cintia Amiñoso, et al.
Pharmacogenetics and Genomics|June 11, 2021
Analytical validation of a laboratory-development multigene pharmacogenetic assayRocío Rosas-Alonso, Javier Queiruga, Pedro Arias, et al.
Cells|November 27, 2021
Expanding the Evidence of a Semi-Dominant Inheritance in <i>GDF2</i> Associated with Pulmonary Arterial HypertensionNatalia Gallego, Alejandro Cruz-Utrilla, Inmaculada Guillén, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 10, 2023
Adult experiences in Beckwith-Wiedemann syndromeWilliam A Drust, Alessandro Mussa, Andrea Gazzin, et al.
Genes|May 28, 2022
Description of Two New Cases of <i>AQP1</i> Related Pulmonary Arterial Hypertension and Review of the LiteratureNatalia Gallego-Zazo, Alejandro Cruz-Utrilla, María Jesús Del Cerro, et al.
Clinical Genetics|October 31, 2023
Genetic and phenotypic findings in 34 novel Spanish patients with DDX3X neurodevelopmental disorderAlejandro Parra, Patricia Pascual, Mario Cazalla, et al.
Revista Espanola De Cardiologia (English Ed.)|July 26, 2016
Molecular Analysis of BMPR2, TBX4, and KCNK3 and Genotype-Phenotype Correlations in Spanish Patients and Families With Idiopathic and Hereditary Pulmonary Arterial HypertensionPaula Navas, Jair Tenorio, Carlos Andrés Quezada, et al.
Clinical Genetics|September 13, 2023
Lamb-Shaffer syndrome: 20 Spanish patients and literature review expands the view of neurodevelopmental disorders caused by SOX5 haploinsufficiencyJair Tenorio-Castano, Ángela Sánchez-Algaba Gómez, Mónica Coronado, et al.
Clinical Genetics|January 11, 2019
MRX93 syndrome (BRWD3 gene): five new patients with novel mutationsJair Tenorio, Pablo Alarcón, Pedro Arias, et al.
Clinical and Translational Science|December 2, 2017
Clinical Implementation of Pharmacogenetic Testing in a Hospital of the Spanish National Health System: Strategy and Experience Over 3 YearsAlberto M Borobia, Irene Dapia, Hoi Y Tong, et al.
Pageof 9