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

María Orera

Showing results (11-20 of 13) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 13 results.
Stem Cell Research|October 19, 2019
Generation of an integration-free iPSC line, ICCSICi006-A, derived from a male Alzheimer's disease patient carrying the PSEN1-G206D mutationEva Díaz-Guerra, Manuel A Oria-Muriel, Elena P Moreno-Jiménez, et al.
Medicina Clinica|April 23, 2018
Recommendations regarding the genetic and immunological study of reproductive dysfunctionMaría Concepción Alonso-Cerezo, Mercedes Calero Ruiz, Venancio Chantada-Abal, et al.
European Journal of Human Genetics : EJHG|April 9, 2015
PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndromeJulián Nevado, Jill A Rosenfeld, Rocío Mena, et al.
Pageof 2

Showing results (11-20 of 13) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 13 results.
Stem Cell Research|October 19, 2019
Generation of an integration-free iPSC line, ICCSICi006-A, derived from a male Alzheimer's disease patient carrying the PSEN1-G206D mutationEva Díaz-Guerra, Manuel A Oria-Muriel, Elena P Moreno-Jiménez, et al.
Medicina Clinica|April 23, 2018
Recommendations regarding the genetic and immunological study of reproductive dysfunctionMaría Concepción Alonso-Cerezo, Mercedes Calero Ruiz, Venancio Chantada-Abal, et al.
European Journal of Human Genetics : EJHG|April 9, 2015
PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndromeJulián Nevado, Jill A Rosenfeld, Rocío Mena, et al.
Pageof 2