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J Trujillo

Showing results (421-430 of 537) with videos related to

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Journal of Medical Genetics|January 15, 2003
Mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa: high prevalence and phenotypic variationS Bernal, C Ayuso, G Antiñolo, et al.
Molecular Genetics and Metabolism Reports|November 23, 2016
Nine-year experience in Gaucher disease diagnosis at the Spanish reference center Fundación Jiménez DíazN V Ortiz-Cabrera, J Gallego-Merlo, C Vélez-Monsalve, et al.
The American Journal of Medicine|August 1, 1989
Refractoriness to chemotherapy and poor survival related to abnormalities of chromosomes 17 and 7 in lymphomaF Cabanillas, S Pathak, G Grant, et al.
Ophthalmic Genetics|July 27, 1999
Retinitis pigmentosa, mental retardation, marked short stature, and brachydactyly in two sibsI Lorda-Sanchez, M J Trujillo, A Gimenez, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: ABCA4. Disease: Stargardt diseaseJana Aguirre-Lamban, R Riveiro-Alvarez, D Cantalapiedra, et al.
Mhealth|February 7, 2024
Design of an innovative digital application to facilitate access to healthy foods in low-income urban settingsEmma C Lewis, Siyao Zhu, Ayoyemi T Oladimeji, et al.
Ultrasonics Sonochemistry|April 27, 2024
Coffee brewing sonoreactor for reducing the time of cold brew from several hours to minutes while maintaining sensory attributesShih-Hao Chiu, Nikunj Naliyadhara, Martin P Bucknall, et al.
European Journal of Neurology|December 4, 2008
Prenatal diagnosis of Huntington disease in maternal plasma: direct and indirect studyA Bustamante-Aragones, M J Trujillo-Tiebas, J Gallego-Merlo, et al.
Molecular Vision|February 6, 2007
Partial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt diseaseR Riveiro-Alvarez, D Valverde, I Lorda-Sanchez, et al.
Human Genetics|June 29, 2007
Gene symbol: CRB1Elena Vallespin, R Riveiro-Alvarez, D Cantalapiedra, et al.
Pageof 54

Showing results (421-430 of 537) with videos related to

Sort By:
Pageof 54
Journal of Medical Genetics|January 15, 2003
Mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa: high prevalence and phenotypic variationS Bernal, C Ayuso, G Antiñolo, et al.
Molecular Genetics and Metabolism Reports|November 23, 2016
Nine-year experience in Gaucher disease diagnosis at the Spanish reference center Fundación Jiménez DíazN V Ortiz-Cabrera, J Gallego-Merlo, C Vélez-Monsalve, et al.
The American Journal of Medicine|August 1, 1989
Refractoriness to chemotherapy and poor survival related to abnormalities of chromosomes 17 and 7 in lymphomaF Cabanillas, S Pathak, G Grant, et al.
Ophthalmic Genetics|July 27, 1999
Retinitis pigmentosa, mental retardation, marked short stature, and brachydactyly in two sibsI Lorda-Sanchez, M J Trujillo, A Gimenez, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: ABCA4. Disease: Stargardt diseaseJana Aguirre-Lamban, R Riveiro-Alvarez, D Cantalapiedra, et al.
Mhealth|February 7, 2024
Design of an innovative digital application to facilitate access to healthy foods in low-income urban settingsEmma C Lewis, Siyao Zhu, Ayoyemi T Oladimeji, et al.
Ultrasonics Sonochemistry|April 27, 2024
Coffee brewing sonoreactor for reducing the time of cold brew from several hours to minutes while maintaining sensory attributesShih-Hao Chiu, Nikunj Naliyadhara, Martin P Bucknall, et al.
European Journal of Neurology|December 4, 2008
Prenatal diagnosis of Huntington disease in maternal plasma: direct and indirect studyA Bustamante-Aragones, M J Trujillo-Tiebas, J Gallego-Merlo, et al.
Molecular Vision|February 6, 2007
Partial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt diseaseR Riveiro-Alvarez, D Valverde, I Lorda-Sanchez, et al.
Human Genetics|June 29, 2007
Gene symbol: CRB1Elena Vallespin, R Riveiro-Alvarez, D Cantalapiedra, et al.
Pageof 54