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M J Trujillo

Showing results (21-30 of 128) with videos related to

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Human Genetics|February 14, 2007
Gene symbol: ABCA4. Disease: Stargardt disease 1. Accession #Hm0536R Riveiro-Alvarez, M J Trujillo, D Cantalapiedra, et al.
Human Genetics|November 28, 2006
Gene symbol: NDP. Disease: Norrie diseaseR Riveiro-Alvarez, M J Trujillo, A Gimenez, et al.
Human Genetics|February 14, 2007
Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hm0534E Vallespin, D Cantalapiedra, M Garcia-Hoyos, et al.
Journal of Assisted Reproduction and Genetics|May 26, 2006
Prenatal diagnosis of 46, XX male fetusM J Trujillo-Tiebas, C González-González, I Lorda-Sánchez, et al.
Anales Del Sistema Sanitario De Navarra|May 3, 2011
[Allergic sensitization profile in the immigrant population living in the central region of Spain]J Dominguez-Ortega, D González de Olano, M J Trujillo, et al.
Human Genetics|October 11, 2008
Gene symbol: RPGR. Disease: Retinitis PigmentosaAscensión Giménez, R Riveiro, M J Trujillo-Tiebas, et al.
Human Mutation|June 30, 2000
Three novel mutations (P215L, T289P, and 3811-2 A-->G) in the rhodopsin gene in autosomal dominant retinitis pigmentosa in Spanish familiesM Martinez-Gimeno, M J Trujillo, I Lorda, et al.
Journal of Investigational Allergology & Clinical Immunology|December 20, 2007
Flare-up-Like phenomenon in a skin prick test after oral challenge with ibuprofenD González de Olano, E González Mancebo, M Gandolfo Cano, et al.
Archivos De La Sociedad Espanola De Oftalmologia|January 11, 2001
[Retinitis pigmentosa, pattern dystrophy and fundus flavimaculatus not related to mutations in rhodopsine, peripherin/RDS and ROM-1 genes]Benítez Del Castillo JM, M J Trujillo, Del Río T, et al.
Human Genetics|February 14, 2007
Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hm0540E Vallespin, D Cantalapiedra, M Garcia-Hoyos, et al.
Pageof 13

Showing results (21-30 of 128) with videos related to

Sort By:
Pageof 13
Human Genetics|February 14, 2007
Gene symbol: ABCA4. Disease: Stargardt disease 1. Accession #Hm0536R Riveiro-Alvarez, M J Trujillo, D Cantalapiedra, et al.
Human Genetics|November 28, 2006
Gene symbol: NDP. Disease: Norrie diseaseR Riveiro-Alvarez, M J Trujillo, A Gimenez, et al.
Human Genetics|February 14, 2007
Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hm0534E Vallespin, D Cantalapiedra, M Garcia-Hoyos, et al.
Journal of Assisted Reproduction and Genetics|May 26, 2006
Prenatal diagnosis of 46, XX male fetusM J Trujillo-Tiebas, C González-González, I Lorda-Sánchez, et al.
Anales Del Sistema Sanitario De Navarra|May 3, 2011
[Allergic sensitization profile in the immigrant population living in the central region of Spain]J Dominguez-Ortega, D González de Olano, M J Trujillo, et al.
Human Genetics|October 11, 2008
Gene symbol: RPGR. Disease: Retinitis PigmentosaAscensión Giménez, R Riveiro, M J Trujillo-Tiebas, et al.
Human Mutation|June 30, 2000
Three novel mutations (P215L, T289P, and 3811-2 A-->G) in the rhodopsin gene in autosomal dominant retinitis pigmentosa in Spanish familiesM Martinez-Gimeno, M J Trujillo, I Lorda, et al.
Journal of Investigational Allergology & Clinical Immunology|December 20, 2007
Flare-up-Like phenomenon in a skin prick test after oral challenge with ibuprofenD González de Olano, E González Mancebo, M Gandolfo Cano, et al.
Archivos De La Sociedad Espanola De Oftalmologia|January 11, 2001
[Retinitis pigmentosa, pattern dystrophy and fundus flavimaculatus not related to mutations in rhodopsine, peripherin/RDS and ROM-1 genes]Benítez Del Castillo JM, M J Trujillo, Del Río T, et al.
Human Genetics|February 14, 2007
Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hm0540E Vallespin, D Cantalapiedra, M Garcia-Hoyos, et al.
Pageof 13