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Raquel Rodríguez-López

Showing results (1-10 of 37) with videos related to

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Revista De Derecho Y Genoma Humano = Law and the Human Genome Review|November 17, 2004
[Human susceptibility to complex diseases. Genetic analysis in large populations]Raquel Rodríguez López
Journal of Human Genetics|March 28, 2014
Association study of common polymorphisms in MSRA, TFAP2B, MC4R, NRXN3, PPARGC1A, TMEM18, SEC16B, HOXB5 and OLFM4 genes with obesity-related traits among Portuguese childrenDavid Albuquerque, Clévio Nóbrega, Raquel Rodríguez-López, et al.
Revista De Derecho Y Genoma Humano = Law and the Human Genome Review|October 29, 2009
[Family law, witness of the analysis of prenatal paternity]Raquel Rodríguez López, Jorge A Marfil, Pedro González Poveda
Molecular Genetics and Genomics : MGG|March 10, 2015
Current review of genetics of human obesity: from molecular mechanisms to an evolutionary perspectiveDavid Albuquerque, Eric Stice, Raquel Rodríguez-López, et al.
Advances in Laboratory Medicine|June 26, 2023
Prenatal genetic diagnosis of monogenic diseasesCarmen Prior-de Castro, Clara Gómez-González, Raquel Rodríguez-López, et al.
Nephrology (Carlton, Vic.)|September 13, 2025
Novel Pathogenic Genotype in SLC12A3 Associated to Gitelman Syndrome: A Case ReportPatricia Tomás-Simó, Antonio Sierra-Rivera, Ana Checa-Ros, et al.
The Journal of Gene Medicine|April 8, 2017
Polymorphisms in the SNRPN gene are associated with obesity susceptibility in a Spanish populationDavid Albuquerque, Licínio Manco, Luz M González, et al.
Dermatology Online Journal|June 21, 2019
Novel PTEN mutation in Cowden syndrome: case report with late diagnosis and non-malignant courseAlvaro Martínez-Doménech, Marta García-Legaz Martínez, Jorge Magdaleno-Tapial, et al.
Ophthalmic Genetics|September 24, 2025
A new genotype of the <i>IDH3A</i> gene causes retinitis pigmentosa, generating functional dyschromatopsia from early childhoodNuria Rosell-Saiz, Antonio Sierra-Rivera, Jordi Tortosa-Carreres, et al.
European Journal of Ophthalmology|January 6, 2022
Twelve-year follow up of a case of autosomal recessive bestrophinopathy with transient resolution of retinal edema in one eyeLidia Remolí Sargues, Clara Monferrer Adsuara, Raquel Rodríguez López, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Revista De Derecho Y Genoma Humano = Law and the Human Genome Review|November 17, 2004
[Human susceptibility to complex diseases. Genetic analysis in large populations]Raquel Rodríguez López
Journal of Human Genetics|March 28, 2014
Association study of common polymorphisms in MSRA, TFAP2B, MC4R, NRXN3, PPARGC1A, TMEM18, SEC16B, HOXB5 and OLFM4 genes with obesity-related traits among Portuguese childrenDavid Albuquerque, Clévio Nóbrega, Raquel Rodríguez-López, et al.
Revista De Derecho Y Genoma Humano = Law and the Human Genome Review|October 29, 2009
[Family law, witness of the analysis of prenatal paternity]Raquel Rodríguez López, Jorge A Marfil, Pedro González Poveda
Molecular Genetics and Genomics : MGG|March 10, 2015
Current review of genetics of human obesity: from molecular mechanisms to an evolutionary perspectiveDavid Albuquerque, Eric Stice, Raquel Rodríguez-López, et al.
Advances in Laboratory Medicine|June 26, 2023
Prenatal genetic diagnosis of monogenic diseasesCarmen Prior-de Castro, Clara Gómez-González, Raquel Rodríguez-López, et al.
Nephrology (Carlton, Vic.)|September 13, 2025
Novel Pathogenic Genotype in SLC12A3 Associated to Gitelman Syndrome: A Case ReportPatricia Tomás-Simó, Antonio Sierra-Rivera, Ana Checa-Ros, et al.
The Journal of Gene Medicine|April 8, 2017
Polymorphisms in the SNRPN gene are associated with obesity susceptibility in a Spanish populationDavid Albuquerque, Licínio Manco, Luz M González, et al.
Dermatology Online Journal|June 21, 2019
Novel PTEN mutation in Cowden syndrome: case report with late diagnosis and non-malignant courseAlvaro Martínez-Doménech, Marta García-Legaz Martínez, Jorge Magdaleno-Tapial, et al.
Ophthalmic Genetics|September 24, 2025
A new genotype of the <i>IDH3A</i> gene causes retinitis pigmentosa, generating functional dyschromatopsia from early childhoodNuria Rosell-Saiz, Antonio Sierra-Rivera, Jordi Tortosa-Carreres, et al.
European Journal of Ophthalmology|January 6, 2022
Twelve-year follow up of a case of autosomal recessive bestrophinopathy with transient resolution of retinal edema in one eyeLidia Remolí Sargues, Clara Monferrer Adsuara, Raquel Rodríguez López, et al.
Pageof 4