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F Prieto

Showing results (111-120 of 157) with videos related to

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Avian Diseases|July 31, 2004
The normal electrocardiogram of the unanesthetized peregrine falcon (Falco peregrinus brookei)R Rodríguez, F Prieto-Montaña, A M Montes, et al.
Human Genetics|September 1, 1993
Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndromeO Bartsch, U König, M B Petersen, et al.
Medicina Clinica|April 20, 1999
[Multiple endocrine neoplasia type 1: genetic study of a large family]C Orellana, R Palasí, F Martínez, et al.
Medicina Clinica|September 14, 1985
[Relation of blood levels of amoxapine and its active metabolites to its pharmacologic response and toxicity]M B Calvo, M J García, J L Pedraz, et al.
Sangre|January 1, 1980
[T-cell leukaemia with receptors for IgG Fc-fraction (author's transl)]J Mayans, F Prieto, G Martin, et al.
Anales De Medicina Interna (Madrid, Spain : 1984)|October 1, 1996
[Recurrent ARDS in varicella pneumonia complicated by disseminated candidiasis in a pregnant woman]F Prieto Valderrey, J L Teja Barbero, T Obeso González, et al.
Clinical Genetics|August 31, 1999
Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in SpainJ M Millán, F Martínez, A Cadroy, et al.
Human Mutation|February 6, 1998
Déjérine-Sottas neuropathy associated with de novo S79P mutation of the peripheral myelin protein 22 (PMP22) geneS Bort, T Sevilla, J García-Planells, et al.
Texas Heart Institute Journal|September 1, 1982
Cor triatriatum with mitral valve disease in adultsM Fuster-Siebert, R Llorens, R Arcas-Meca, et al.
American Journal of Human Genetics|July 27, 1999
Mutation of the XNP/ATR-X gene in a family with severe mental retardation, spastic paraplegia and skewed pattern of X inactivation: demonstration that the mutation is involved in the inactivation biasA M Lossi, J M Millán, L Villard, et al.
Pageof 16

Showing results (111-120 of 157) with videos related to

Sort By:
Pageof 16
Avian Diseases|July 31, 2004
The normal electrocardiogram of the unanesthetized peregrine falcon (Falco peregrinus brookei)R Rodríguez, F Prieto-Montaña, A M Montes, et al.
Human Genetics|September 1, 1993
Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndromeO Bartsch, U König, M B Petersen, et al.
Medicina Clinica|April 20, 1999
[Multiple endocrine neoplasia type 1: genetic study of a large family]C Orellana, R Palasí, F Martínez, et al.
Medicina Clinica|September 14, 1985
[Relation of blood levels of amoxapine and its active metabolites to its pharmacologic response and toxicity]M B Calvo, M J García, J L Pedraz, et al.
Sangre|January 1, 1980
[T-cell leukaemia with receptors for IgG Fc-fraction (author's transl)]J Mayans, F Prieto, G Martin, et al.
Anales De Medicina Interna (Madrid, Spain : 1984)|October 1, 1996
[Recurrent ARDS in varicella pneumonia complicated by disseminated candidiasis in a pregnant woman]F Prieto Valderrey, J L Teja Barbero, T Obeso González, et al.
Clinical Genetics|August 31, 1999
Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in SpainJ M Millán, F Martínez, A Cadroy, et al.
Human Mutation|February 6, 1998
Déjérine-Sottas neuropathy associated with de novo S79P mutation of the peripheral myelin protein 22 (PMP22) geneS Bort, T Sevilla, J García-Planells, et al.
Texas Heart Institute Journal|September 1, 1982
Cor triatriatum with mitral valve disease in adultsM Fuster-Siebert, R Llorens, R Arcas-Meca, et al.
American Journal of Human Genetics|July 27, 1999
Mutation of the XNP/ATR-X gene in a family with severe mental retardation, spastic paraplegia and skewed pattern of X inactivation: demonstration that the mutation is involved in the inactivation biasA M Lossi, J M Millán, L Villard, et al.
Pageof 16