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M J Trujillo

Showing results (41-50 of 128) with videos related to

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Human Genetics|February 14, 2007
Gene symbol: ABCA4. Disease: Stargardt disease 1. Accession #Hm0538R Riveiro-Alvarez, J Aguirre, M J Trujillo, et al.
Medicina Clinica|January 6, 2001
[Asp-190-Tyr mutation in the rhodopsin gene in a Spanish family with autosomic dominant pigmentary retinosis]M Martínez Gimeno, M J Trujillo, B García Sandoval, et al.
Human Genetics|April 4, 2008
Gene symbol: BEST1. Disease: Best macular dystrophySusana Maia-Lopes, M Castelo-Branco, E Silva, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: COL7A1. Disease: Epidermolysis bullosa dystrophicaMarta Garcia, M J Escamez, N Cuadrado-Corrales, et al.
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: CHM. Disease: choroideraemiaCristina Villaverde, M J Trujillo-Tiebas, M Garcia-Hoyos, et al.
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: EPM2A. Disease: Lafora progressive myoclonus epilepsyM J Trujillo-Tiebas, M Fenollar-Cortés, P Gómez-Garré, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: COL7A1. Disease: Epidermolysis bullosa dystrophicaNatividad Cuadrado-Corrales, M Garcia, M J Escamez, et al.
Human Genetics|April 4, 2008
Gene symbol: BEST1. Disease: Best macular dystrophySusana Maia-Lopes, M Castelo-Branco, E Silva, et al.
Allergologia Et Immunopathologia|August 2, 2016
Comparison of two diagnostic techniques, skin-prick test and component resolved diagnosis in the follow-up of a cohort of paediatric patients with pollinosis. Multicentre pilot study in a highly exposed allergenic areaE González-Mancebo, J Domínguez-Ortega, S Blanco-Bermejo, et al.
Human Mutation|July 29, 1999
Identification of three novel mutations in the MYO7A geneJ M Cuevas, C Espinós, J M Millán, et al.
Pageof 13

Showing results (41-50 of 128) with videos related to

Sort By:
Pageof 13
Human Genetics|February 14, 2007
Gene symbol: ABCA4. Disease: Stargardt disease 1. Accession #Hm0538R Riveiro-Alvarez, J Aguirre, M J Trujillo, et al.
Medicina Clinica|January 6, 2001
[Asp-190-Tyr mutation in the rhodopsin gene in a Spanish family with autosomic dominant pigmentary retinosis]M Martínez Gimeno, M J Trujillo, B García Sandoval, et al.
Human Genetics|April 4, 2008
Gene symbol: BEST1. Disease: Best macular dystrophySusana Maia-Lopes, M Castelo-Branco, E Silva, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: COL7A1. Disease: Epidermolysis bullosa dystrophicaMarta Garcia, M J Escamez, N Cuadrado-Corrales, et al.
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: CHM. Disease: choroideraemiaCristina Villaverde, M J Trujillo-Tiebas, M Garcia-Hoyos, et al.
Human Genetics|September 20, 2007
Novel human pathological mutations. Gene symbol: EPM2A. Disease: Lafora progressive myoclonus epilepsyM J Trujillo-Tiebas, M Fenollar-Cortés, P Gómez-Garré, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: COL7A1. Disease: Epidermolysis bullosa dystrophicaNatividad Cuadrado-Corrales, M Garcia, M J Escamez, et al.
Human Genetics|April 4, 2008
Gene symbol: BEST1. Disease: Best macular dystrophySusana Maia-Lopes, M Castelo-Branco, E Silva, et al.
Allergologia Et Immunopathologia|August 2, 2016
Comparison of two diagnostic techniques, skin-prick test and component resolved diagnosis in the follow-up of a cohort of paediatric patients with pollinosis. Multicentre pilot study in a highly exposed allergenic areaE González-Mancebo, J Domínguez-Ortega, S Blanco-Bermejo, et al.
Human Mutation|July 29, 1999
Identification of three novel mutations in the MYO7A geneJ M Cuevas, C Espinós, J M Millán, et al.
Pageof 13