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C Ayuso

Showing results (71-80 of 264) with videos related to

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Ophthalmic Genetics|September 1, 1996
G106R rhodopsin mutation is also present in Spanish ADRP patientsC Ayuso, C Reig, B Garcia-Sandoval, et al.
International Journal of Laboratory Hematology|November 27, 2012
Utility of new mature erythrocyte and reticulocyte indices in screening for iron-deficiency anemia in a pediatric populationV Osta, M S Caldirola, M Fernandez, et al.
Human Mutation|January 8, 2000
Three novel RDS-peripherin mutations (689delT, 857del17, G208D) in Spanish families affected with autosomal dominant retinal degenerations. Mutations in brief no. 147. OnlineM J Trujillo, J Bueno, A Osorio, et al.
Human Mutation|April 1, 1998
Novel mutations in the TIGR gene in early and late onset open angle glaucomaF C Mansergh, P F Kenna, C Ayuso, et al.
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.
Gastroenterology|September 1, 1995
Treatment of hepatocellular carcinoma with tamoxifen: a double-blind placebo-controlled trial in 120 patientsA Castells, J Bruix, C Brú, et al.
Human Genetics|February 14, 2007
Gene symbol: ABCA4. Disease: Stargardt disease 1. Accession #Hs0512R Riveiro-Alvarez, M J Trujillo, D Cantalapiedra, 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.
Pageof 27

Showing results (71-80 of 264) with videos related to

Sort By:
Pageof 27
Ophthalmic Genetics|September 1, 1996
G106R rhodopsin mutation is also present in Spanish ADRP patientsC Ayuso, C Reig, B Garcia-Sandoval, et al.
International Journal of Laboratory Hematology|November 27, 2012
Utility of new mature erythrocyte and reticulocyte indices in screening for iron-deficiency anemia in a pediatric populationV Osta, M S Caldirola, M Fernandez, et al.
Human Mutation|January 8, 2000
Three novel RDS-peripherin mutations (689delT, 857del17, G208D) in Spanish families affected with autosomal dominant retinal degenerations. Mutations in brief no. 147. OnlineM J Trujillo, J Bueno, A Osorio, et al.
Human Mutation|April 1, 1998
Novel mutations in the TIGR gene in early and late onset open angle glaucomaF C Mansergh, P F Kenna, C Ayuso, et al.
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.
Gastroenterology|September 1, 1995
Treatment of hepatocellular carcinoma with tamoxifen: a double-blind placebo-controlled trial in 120 patientsA Castells, J Bruix, C Brú, et al.
Human Genetics|February 14, 2007
Gene symbol: ABCA4. Disease: Stargardt disease 1. Accession #Hs0512R Riveiro-Alvarez, M J Trujillo, D Cantalapiedra, 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.
Pageof 27