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D Valverde

Showing results (51-60 of 69) with videos related to

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Human Genetics|January 1, 1996
A novel mutation in exon 17 of the beta-subunit of rod phosphodiesterase in two RP sisters of a consanguineous familyD Valverde, T Solans, D Grinberg, 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.
Clinical Genetics|November 1, 1996
Autosomal recessive retinitis pigmentosa in Spain: evaluation of four genes and two loci involved in the diseaseM Bayés, A Martínez-Mir, D Valverde, et al.
Revista Espanola De Enfermedades Digestivas|March 29, 2006
[Reply to "anal prolapse of a sigmoid lipoma"]S Pérez-Holanda, D Valverde, G Urdiales, et al.
Human Mutation|January 1, 1996
Identification of a novel R552O mutation in exon 13 of the beta-subunit of rod phosphodiesterase gene in a Spanish family with autosomal recessive retinitis pigmentosaD Valverde, M Baiget, R Seminago, et al.
Revista Espanola De Enfermedades Digestivas|October 24, 2008
[Pneumoperitoneum with intramural gas in a bowel segment]S Pérez-Holanda, L M López-Negrete, J A Fernández, et al.
Human Genetics|June 1, 1997
Putative association of a mutant ROM1 allele with retinitis pigmentosaA Martínez-Mir, C Vilela, M Bayés, et al.
Revista Espanola De Enfermedades Digestivas|September 24, 2008
[Preoperative workup to assess indication for laparoscopic treatment in gastroesophageal reflux disease]S Pérez-Holanda, G L Urdiales, J A Fernández, et al.
Human Mutation|January 29, 2000
Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. OnlineM G Miano, D Valverde, T Solans, et al.
Human Mutation|February 14, 2006
Mutation profile of the MYO7A gene in Spanish patients with Usher syndrome type IT Jaijo, E Aller, S Oltra, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
Human Genetics|January 1, 1996
A novel mutation in exon 17 of the beta-subunit of rod phosphodiesterase in two RP sisters of a consanguineous familyD Valverde, T Solans, D Grinberg, 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.
Clinical Genetics|November 1, 1996
Autosomal recessive retinitis pigmentosa in Spain: evaluation of four genes and two loci involved in the diseaseM Bayés, A Martínez-Mir, D Valverde, et al.
Revista Espanola De Enfermedades Digestivas|March 29, 2006
[Reply to "anal prolapse of a sigmoid lipoma"]S Pérez-Holanda, D Valverde, G Urdiales, et al.
Human Mutation|January 1, 1996
Identification of a novel R552O mutation in exon 13 of the beta-subunit of rod phosphodiesterase gene in a Spanish family with autosomal recessive retinitis pigmentosaD Valverde, M Baiget, R Seminago, et al.
Revista Espanola De Enfermedades Digestivas|October 24, 2008
[Pneumoperitoneum with intramural gas in a bowel segment]S Pérez-Holanda, L M López-Negrete, J A Fernández, et al.
Human Genetics|June 1, 1997
Putative association of a mutant ROM1 allele with retinitis pigmentosaA Martínez-Mir, C Vilela, M Bayés, et al.
Revista Espanola De Enfermedades Digestivas|September 24, 2008
[Preoperative workup to assess indication for laparoscopic treatment in gastroesophageal reflux disease]S Pérez-Holanda, G L Urdiales, J A Fernández, et al.
Human Mutation|January 29, 2000
Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. OnlineM G Miano, D Valverde, T Solans, et al.
Human Mutation|February 14, 2006
Mutation profile of the MYO7A gene in Spanish patients with Usher syndrome type IT Jaijo, E Aller, S Oltra, et al.
Pageof 7