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

F Abidi

Showing results (31-40 of 34) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 34 results.
Journal of Medical Genetics|April 16, 1999
Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndromeL Villard, M C Bonino, F Abidi, et al.
Genomics|December 1, 1991
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28D Schlessinger, R D Little, D Freije, et al.
Clinical Genetics|May 9, 2014
Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X)M J Basehore, R Michaelson-Cohen, E Levy-Lahad, et al.
Human Genetics|December 22, 1998
Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1N Rahman, F Abidi, D Ford, et al.
Pageof 4

Showing results (31-40 of 34) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 34 results.
Journal of Medical Genetics|April 16, 1999
Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndromeL Villard, M C Bonino, F Abidi, et al.
Genomics|December 1, 1991
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28D Schlessinger, R D Little, D Freije, et al.
Clinical Genetics|May 9, 2014
Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X)M J Basehore, R Michaelson-Cohen, E Levy-Lahad, et al.
Human Genetics|December 22, 1998
Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1N Rahman, F Abidi, D Ford, et al.
Pageof 4