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C Gonzalez-Gonzalez

Showing results (1-10 of 11) with videos related to

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Public Health|February 4, 2021
Factors associated with pain at the end-of-life among older adults in MexicoR Samper-Ternent, C Gonzalez-Gonzalez, J D Zazueta, et al.
Revista De Neurologia|September 19, 2007
[Giant arachnoid granulations]C Gonzalez-Gonzalez, E Alventosa-Fernandez, C Villar-Van den Weygaert, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|April 5, 2014
Treatment of persistent/medically refractory covert hepatic encephalopathy with the molecular adsorbent recirculating systemMichael D Leise, Nelson Leung, Ziad El-Zoghby, et al.
Ophthalmic Genetics|November 30, 2021
Novel <i>CHRDL1</i> mutation causing X-linked megalocornea in a family with mild anterior segment manifestations in carrier femalesRocio Arce-Gonzalez, Oscar F Chacon-Camacho, Alejandro Navas-Perez, et al.
European Journal of Neurology|December 4, 2008
Prenatal diagnosis of Huntington disease in maternal plasma: direct and indirect studyA Bustamante-Aragones, M J Trujillo-Tiebas, J Gallego-Merlo, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 11, 2008
Foetal sex determination in maternal blood from the seventh week of gestation and its role in diagnosing haemophilia in the foetuses of female carriersA Bustamante-Aragones, M Rodriguez de Alba, C Gonzalez-Gonzalez, et al.
American Journal of Medical Genetics|February 24, 2001
Cryptic 6q subtelomeric deletion associated with a paracentric inversion in a mildly retarded childI Lorda-Sanchez, I Lopez-Pajares, M C Roche, et al.
Ophthalmic Genetics|January 3, 2001
Ser186Pro mutation of RHO gene in a Spanish autosomal dominant retinitis pigmentosa (ADRP) familyM J Trujillo, B Garcia-Sandoval, I Lorda-Sanchez, et al.
Fetal Diagnosis and Therapy|February 15, 2001
Chromosomal mosaicism for isochromosome 11q confined to CVS direct preparationsR Sanz, I Lorda-Sanchez, J M Fernández-Moya, et al.
Genetic Counseling (Geneva, Switzerland)|August 2, 2002
Aniridia as part of a WAGR syndrome in a girl whose brother presented hypospadiasI Lorda-Sanchez, R Sanz, M A Diaz-Guillen, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Public Health|February 4, 2021
Factors associated with pain at the end-of-life among older adults in MexicoR Samper-Ternent, C Gonzalez-Gonzalez, J D Zazueta, et al.
Revista De Neurologia|September 19, 2007
[Giant arachnoid granulations]C Gonzalez-Gonzalez, E Alventosa-Fernandez, C Villar-Van den Weygaert, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|April 5, 2014
Treatment of persistent/medically refractory covert hepatic encephalopathy with the molecular adsorbent recirculating systemMichael D Leise, Nelson Leung, Ziad El-Zoghby, et al.
Ophthalmic Genetics|November 30, 2021
Novel <i>CHRDL1</i> mutation causing X-linked megalocornea in a family with mild anterior segment manifestations in carrier femalesRocio Arce-Gonzalez, Oscar F Chacon-Camacho, Alejandro Navas-Perez, et al.
European Journal of Neurology|December 4, 2008
Prenatal diagnosis of Huntington disease in maternal plasma: direct and indirect studyA Bustamante-Aragones, M J Trujillo-Tiebas, J Gallego-Merlo, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 11, 2008
Foetal sex determination in maternal blood from the seventh week of gestation and its role in diagnosing haemophilia in the foetuses of female carriersA Bustamante-Aragones, M Rodriguez de Alba, C Gonzalez-Gonzalez, et al.
American Journal of Medical Genetics|February 24, 2001
Cryptic 6q subtelomeric deletion associated with a paracentric inversion in a mildly retarded childI Lorda-Sanchez, I Lopez-Pajares, M C Roche, et al.
Ophthalmic Genetics|January 3, 2001
Ser186Pro mutation of RHO gene in a Spanish autosomal dominant retinitis pigmentosa (ADRP) familyM J Trujillo, B Garcia-Sandoval, I Lorda-Sanchez, et al.
Fetal Diagnosis and Therapy|February 15, 2001
Chromosomal mosaicism for isochromosome 11q confined to CVS direct preparationsR Sanz, I Lorda-Sanchez, J M Fernández-Moya, et al.
Genetic Counseling (Geneva, Switzerland)|August 2, 2002
Aniridia as part of a WAGR syndrome in a girl whose brother presented hypospadiasI Lorda-Sanchez, R Sanz, M A Diaz-Guillen, et al.
Pageof 2