Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C Ayuso

Showing results (51-60 of 264) with videos related to

Pageof 27
Sort By:
Medicina Clinica|March 1, 1997
[A clinical, cytogenetic and molecular study of 10 patients with the Prader-Willi syndrome]A Barabash, M Robledo, R Sanz, et al.
Human Genetics|August 1, 1995
Somatic stability in chorionic villi samples and other Huntington fetal tissuesJ Benitez, M Robledo, C Ramos, et al.
Anales Espanoles De Pediatria|September 1, 1992
[Modification of the calculation of risk factors in women, possible carriers of Duchenne muscular dystrophy, based on CPK levels]M Villamar López, J Azpeitia González, C Ayuso García, et al.
Revista Clinica Espanola|June 15, 1981
[New case of 48,XXYY syndrome]M C Ayuso García, M C Ramos Corrales, M J Bello González, et al.
Human Genetics|September 1, 1994
Identification of a novel rhodopsin mutation (Met-44-Thr) in a simplex case of retinitis pigmentosaC Reig, J Antich, E Gean, et al.
Anales Espanoles De Pediatria|September 1, 1981
[Partial trisomy 11q;22q (author's transl)]J Benítez, C Ayuso, J García Aparicio, 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.
European Radiology|June 17, 1999
Atypical retroperitoneal fibrosis: MRI findingsJ R Ayuso, A Garcia-Criado, T M Caralt, et al.
Actas Dermo-Sifiliograficas|November 29, 2017
Genetic diagnosis of epidermolysis bullosa: recommendations from an expert Spanish research groupC Sánchez-Jimeno, M J Escámez, C Ayuso, et al.
Human Mutation|June 1, 2001
Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosaM Martinez-Gimeno, M Maseras, M Baiget, et al.
Pageof 27

Showing results (51-60 of 264) with videos related to

Sort By:
Pageof 27
Medicina Clinica|March 1, 1997
[A clinical, cytogenetic and molecular study of 10 patients with the Prader-Willi syndrome]A Barabash, M Robledo, R Sanz, et al.
Human Genetics|August 1, 1995
Somatic stability in chorionic villi samples and other Huntington fetal tissuesJ Benitez, M Robledo, C Ramos, et al.
Anales Espanoles De Pediatria|September 1, 1992
[Modification of the calculation of risk factors in women, possible carriers of Duchenne muscular dystrophy, based on CPK levels]M Villamar López, J Azpeitia González, C Ayuso García, et al.
Revista Clinica Espanola|June 15, 1981
[New case of 48,XXYY syndrome]M C Ayuso García, M C Ramos Corrales, M J Bello González, et al.
Human Genetics|September 1, 1994
Identification of a novel rhodopsin mutation (Met-44-Thr) in a simplex case of retinitis pigmentosaC Reig, J Antich, E Gean, et al.
Anales Espanoles De Pediatria|September 1, 1981
[Partial trisomy 11q;22q (author's transl)]J Benítez, C Ayuso, J García Aparicio, 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.
European Radiology|June 17, 1999
Atypical retroperitoneal fibrosis: MRI findingsJ R Ayuso, A Garcia-Criado, T M Caralt, et al.
Actas Dermo-Sifiliograficas|November 29, 2017
Genetic diagnosis of epidermolysis bullosa: recommendations from an expert Spanish research groupC Sánchez-Jimeno, M J Escámez, C Ayuso, et al.
Human Mutation|June 1, 2001
Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosaM Martinez-Gimeno, M Maseras, M Baiget, et al.
Pageof 27