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I Lorda-Sánchez

Showing results (1-10 of 15) with videos related to

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Medicina Clinica|June 5, 1998
[Achondroplasia: molecular study of 28 patients]C Climent, I Lorda-Sánchez, M Urioste, et al.
Human Genetics|February 1, 1996
Severe congenital limb deficiencies, vertebral hypersegmentation, absent thymus and mirror polydactyly: a defect expression of a developmental control gene?M Urioste, I Lorda-Sánchez, M Blanco, et al.
Journal of Neurogenetics|March 26, 2008
Two non-contiguous duplications in the DMD gene in a Spanish familyM Fenollar-Cortés, J Gallego-Merlo, M J Trujillo-Tiebas, et al.
American Journal of Medical Genetics|February 11, 1997
Tetrasomy 5p mosaicism due to an extra i(5p) in a severely affected girlI Lorda-Sánchez, A Villa, M Urioste, 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.
American Journal of Medical Genetics|October 23, 1995
Distal deletion of chromosome 13 in a child with the "opitz" GBBB syndromeM Urioste, I Arroyo, A Villa, et al.
Archivos De La Sociedad Espanola De Oftalmologia|April 20, 2013
Guidelines for genetic study of aniridiaF Blanco-Kelly, C Villaverde-Montero, I Lorda-Sánchez, et al.
American Journal of Medical Genetics|February 11, 1997
Proximal partial 5p trisomy resulting from a maternal (19;5) insertionI Lorda-Sánchez, M Urioste, A Villa, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
New approach for the refinement of the location of the X-chromosome breakpoint in a previously described female patient with choroideremia carrying a X;4 translocationM García-Hoyos, R Sanz, D Diego-Alvarez, et al.
Journal of Assisted Reproduction and Genetics|October 1, 2009
Prenatal diagnosis of skeletal dysplasia due to FGFR3 gene mutations: a 9-year experience : prenatal diagnosis in FGFR3 geneM J Trujillo-Tiebas, M Fenollar-Cortés, I Lorda-Sánchez, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Medicina Clinica|June 5, 1998
[Achondroplasia: molecular study of 28 patients]C Climent, I Lorda-Sánchez, M Urioste, et al.
Human Genetics|February 1, 1996
Severe congenital limb deficiencies, vertebral hypersegmentation, absent thymus and mirror polydactyly: a defect expression of a developmental control gene?M Urioste, I Lorda-Sánchez, M Blanco, et al.
Journal of Neurogenetics|March 26, 2008
Two non-contiguous duplications in the DMD gene in a Spanish familyM Fenollar-Cortés, J Gallego-Merlo, M J Trujillo-Tiebas, et al.
American Journal of Medical Genetics|February 11, 1997
Tetrasomy 5p mosaicism due to an extra i(5p) in a severely affected girlI Lorda-Sánchez, A Villa, M Urioste, 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.
American Journal of Medical Genetics|October 23, 1995
Distal deletion of chromosome 13 in a child with the "opitz" GBBB syndromeM Urioste, I Arroyo, A Villa, et al.
Archivos De La Sociedad Espanola De Oftalmologia|April 20, 2013
Guidelines for genetic study of aniridiaF Blanco-Kelly, C Villaverde-Montero, I Lorda-Sánchez, et al.
American Journal of Medical Genetics|February 11, 1997
Proximal partial 5p trisomy resulting from a maternal (19;5) insertionI Lorda-Sánchez, M Urioste, A Villa, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
New approach for the refinement of the location of the X-chromosome breakpoint in a previously described female patient with choroideremia carrying a X;4 translocationM García-Hoyos, R Sanz, D Diego-Alvarez, et al.
Journal of Assisted Reproduction and Genetics|October 1, 2009
Prenatal diagnosis of skeletal dysplasia due to FGFR3 gene mutations: a 9-year experience : prenatal diagnosis in FGFR3 geneM J Trujillo-Tiebas, M Fenollar-Cortés, I Lorda-Sánchez, et al.
Pageof 2