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F Prieto

Showing results (131-140 of 157) with videos related to

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Cytogenetic and Genome Research|February 18, 2006
Recombinant X chromosome in a prenatal diagnosisC Orellana, L Badía, F Martínez, et al.
Cancer Genetics and Cytogenetics|April 18, 1998
Pediatric brain tumors: loss of heterozygosity at 17p and TP53 gene mutationsC Orellana, M Hernandez-Martí, F Martínez, et al.
Medicina Intensiva|June 4, 2011
[Pulmonary thromboembolism and congenital absence of the inferior vena cava]J Villegas-Del Ojo, E Moreno-Millán, J Málaga-Gil, et al.
Cancer Genetics and Cytogenetics|November 1, 1992
Cytogenetic studies in 112 cases of untreated myelodysplastic syndromesF Solé, F Prieto, L Badia, et al.
American Journal of Human Genetics|July 1, 1997
Phenotype correlation and intergenerational dynamics of the Friedreich ataxia GAA trinucleotide repeatE Monrós, M D Moltó, F Martínez, et al.
Medicina Intensiva|September 27, 2012
[Utility of diffusion-weighted magnetic resonance imaging in severe focal traumatic brain injuries]F Prieto-Valderrey, J R Muñiz-Montes, J A López-García, et al.
Revista Clinica Espanola|April 15, 1980
[Primary nodular lymphoma of the left pararectal space]J Hebrero, J Segura, F Prieto, et al.
Journal of Medical Genetics|October 3, 1999
Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCRR Valero, G Marfany, R Gil-Benso, et al.
Scientific Reports|December 12, 2022
Shallow magmatic intrusion evolution below La Palma before and during the 2021 eruptionJosé Fernández, Joaquin Escayo, Antonio G Camacho, et al.
Human Mutation|January 1, 1994
Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosaG Grüning, J M Millan, M Meins, et al.
Pageof 16

Showing results (131-140 of 157) with videos related to

Sort By:
Pageof 16
Cytogenetic and Genome Research|February 18, 2006
Recombinant X chromosome in a prenatal diagnosisC Orellana, L Badía, F Martínez, et al.
Cancer Genetics and Cytogenetics|April 18, 1998
Pediatric brain tumors: loss of heterozygosity at 17p and TP53 gene mutationsC Orellana, M Hernandez-Martí, F Martínez, et al.
Medicina Intensiva|June 4, 2011
[Pulmonary thromboembolism and congenital absence of the inferior vena cava]J Villegas-Del Ojo, E Moreno-Millán, J Málaga-Gil, et al.
Cancer Genetics and Cytogenetics|November 1, 1992
Cytogenetic studies in 112 cases of untreated myelodysplastic syndromesF Solé, F Prieto, L Badia, et al.
American Journal of Human Genetics|July 1, 1997
Phenotype correlation and intergenerational dynamics of the Friedreich ataxia GAA trinucleotide repeatE Monrós, M D Moltó, F Martínez, et al.
Medicina Intensiva|September 27, 2012
[Utility of diffusion-weighted magnetic resonance imaging in severe focal traumatic brain injuries]F Prieto-Valderrey, J R Muñiz-Montes, J A López-García, et al.
Revista Clinica Espanola|April 15, 1980
[Primary nodular lymphoma of the left pararectal space]J Hebrero, J Segura, F Prieto, et al.
Journal of Medical Genetics|October 3, 1999
Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCRR Valero, G Marfany, R Gil-Benso, et al.
Scientific Reports|December 12, 2022
Shallow magmatic intrusion evolution below La Palma before and during the 2021 eruptionJosé Fernández, Joaquin Escayo, Antonio G Camacho, et al.
Human Mutation|January 1, 1994
Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosaG Grüning, J M Millan, M Meins, et al.
Pageof 16