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Graciela Moya

Showing results (1-10 of 8) with videos related to

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Archivos Argentinos De Pediatria|July 12, 2016
Rights of persons with conditions associated with disability: current legal frameworkGraciela Moya
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 2, 2002
Adding another "hatched pink" chromosomeJose Maria Sánchez, Graciela Moya
Medicina|April 23, 2002
[Cadasil: a case with molecular diagnosis]María C Zurrú, Ignacio Casas Parera, Graciela Moya, et al.
Journal of Medical Genetics|January 16, 2007
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophyJulie Desir, Graciela Moya, Orit Reish, et al.
Ophthalmic Genetics|March 12, 2019
Clinical features and possible founder mutation of the 8bp duplication mutation in the SLC4A11 gene causing corneal dystrophy and perceptive deafness in three South American familiesPablo T Romero, Rodrigo Donoso, Pamela López, et al.
Clinical Therapeutics|August 13, 2020
Challenges and Opportunities for Clinical Pharmacogenetic Research Studies in Resource-limited Settings: Conclusions From the Council for International Organizations of Medical Sciences-Ibero-American Network of Pharmacogenetics and Pharmacogenomics MeetingEva Peñas-LLedó, Enrique Terán, Marta Sosa-Macías, et al.
Pharmacogenomics|August 2, 2023
Pharmacogenetics: ethnicity, treatment and health in Latin American populationsMartha Sosa-Macías, Ingrid Fricke-Galindo, Humberto Fariñas, et al.
Nature Genetics|November 15, 2016
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomaliesClaire Redin, Harrison Brand, Ryan L Collins, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Archivos Argentinos De Pediatria|July 12, 2016
Rights of persons with conditions associated with disability: current legal frameworkGraciela Moya
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 2, 2002
Adding another "hatched pink" chromosomeJose Maria Sánchez, Graciela Moya
Medicina|April 23, 2002
[Cadasil: a case with molecular diagnosis]María C Zurrú, Ignacio Casas Parera, Graciela Moya, et al.
Journal of Medical Genetics|January 16, 2007
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophyJulie Desir, Graciela Moya, Orit Reish, et al.
Ophthalmic Genetics|March 12, 2019
Clinical features and possible founder mutation of the 8bp duplication mutation in the SLC4A11 gene causing corneal dystrophy and perceptive deafness in three South American familiesPablo T Romero, Rodrigo Donoso, Pamela López, et al.
Clinical Therapeutics|August 13, 2020
Challenges and Opportunities for Clinical Pharmacogenetic Research Studies in Resource-limited Settings: Conclusions From the Council for International Organizations of Medical Sciences-Ibero-American Network of Pharmacogenetics and Pharmacogenomics MeetingEva Peñas-LLedó, Enrique Terán, Marta Sosa-Macías, et al.
Pharmacogenomics|August 2, 2023
Pharmacogenetics: ethnicity, treatment and health in Latin American populationsMartha Sosa-Macías, Ingrid Fricke-Galindo, Humberto Fariñas, et al.
Nature Genetics|November 15, 2016
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomaliesClaire Redin, Harrison Brand, Ryan L Collins, et al.
Pageof 1