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

A Belinchón

Showing results (1-10 of 5) with videos related to

Pageof 1
Sort By:
Revista Espanola De Anestesiologia Y Reanimacion|March 1, 1989
[Our experience in fiberoptic intubation in anesthesia]A Cartelle, A Belinchón
Acta Otorrinolaringologica Espanola|April 18, 2006
[Ménière's disease and migraine]L Pérez López, A Belinchón de Diego, A Bermell Carrión, et al.
Acta Otorrinolaringologica Espanola|April 12, 2005
[Kinetic tests representativity in vestibular function]A Belinchón de Diego, A Garcia Piñero, L Pérez López, et al.
Placenta|April 24, 2009
CDKN1C mutations in HELLP/preeclamptic mothers of Beckwith-Wiedemann Syndrome (BWS) patientsV Romanelli, A Belinchón, A Campos-Barros, et al.
Clinical Genetics|January 10, 2017
Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasiaJ Barraza-García, C I Rivera-Pedroza, A Hisado-Oliva, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Revista Espanola De Anestesiologia Y Reanimacion|March 1, 1989
[Our experience in fiberoptic intubation in anesthesia]A Cartelle, A Belinchón
Acta Otorrinolaringologica Espanola|April 18, 2006
[Ménière's disease and migraine]L Pérez López, A Belinchón de Diego, A Bermell Carrión, et al.
Acta Otorrinolaringologica Espanola|April 12, 2005
[Kinetic tests representativity in vestibular function]A Belinchón de Diego, A Garcia Piñero, L Pérez López, et al.
Placenta|April 24, 2009
CDKN1C mutations in HELLP/preeclamptic mothers of Beckwith-Wiedemann Syndrome (BWS) patientsV Romanelli, A Belinchón, A Campos-Barros, et al.
Clinical Genetics|January 10, 2017
Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasiaJ Barraza-García, C I Rivera-Pedroza, A Hisado-Oliva, et al.
Pageof 1