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Wilmer Delgado-Luengo

Showing results (1-10 of 6) with videos related to

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Investigacion Clinica|February 15, 2008
[Autism, chromosome 15 and the GAbaergic dysfunction hypothesis]Ernesto Solís-Añez, Wilmer Delgado-Luengo, María Luisa Hernández
Community Genetics|November 13, 2004
Medical genetics in Zulia, a State of VenezuelaSandra González-Ferrer, Lennie Pineda-Bernal, Wilmer Delgado-Luengo, et al.
Investigacion Clinica|June 26, 2018
PAGOD syndrome and vascular anomalies: is a defect embryonic angiogenesis? A case report and reviewWilmer Delgado-Luengo, Herminia Fleitas-Cabello, Ernesto Solís-Añez, et al.
Archivos Argentinos De Pediatria|March 3, 2015
[Double mutant alleles in the EXT1 gene not previously reported in a teenager with hereditary multiple exostoses]Francisco Cammarata-Scalisi, Mónica Cozar, Daniel Grinberg, et al.
American Journal of Medical Genetics|November 20, 2002
Del(1)(q23) in a patient with Hutchinson-Gilford progeriaWilmer Delgado Luengo, Augusto Rojas Martínez, Rocío Ortíz López, et al.
Investigacion Clinica|June 30, 2007
[Molecular analysis of the GABRB3 gene in autistic patients: an exploratory study]Ernesto Solís-Añez, Wilmer Delgado-Luengo, Lisbeth Borjas-Fuentes, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Investigacion Clinica|February 15, 2008
[Autism, chromosome 15 and the GAbaergic dysfunction hypothesis]Ernesto Solís-Añez, Wilmer Delgado-Luengo, María Luisa Hernández
Community Genetics|November 13, 2004
Medical genetics in Zulia, a State of VenezuelaSandra González-Ferrer, Lennie Pineda-Bernal, Wilmer Delgado-Luengo, et al.
Investigacion Clinica|June 26, 2018
PAGOD syndrome and vascular anomalies: is a defect embryonic angiogenesis? A case report and reviewWilmer Delgado-Luengo, Herminia Fleitas-Cabello, Ernesto Solís-Añez, et al.
Archivos Argentinos De Pediatria|March 3, 2015
[Double mutant alleles in the EXT1 gene not previously reported in a teenager with hereditary multiple exostoses]Francisco Cammarata-Scalisi, Mónica Cozar, Daniel Grinberg, et al.
American Journal of Medical Genetics|November 20, 2002
Del(1)(q23) in a patient with Hutchinson-Gilford progeriaWilmer Delgado Luengo, Augusto Rojas Martínez, Rocío Ortíz López, et al.
Investigacion Clinica|June 30, 2007
[Molecular analysis of the GABRB3 gene in autistic patients: an exploratory study]Ernesto Solís-Añez, Wilmer Delgado-Luengo, Lisbeth Borjas-Fuentes, et al.
Pageof 1