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

I Cherkaoui Jaouad

Showing results (1-10 of 6) with videos related to

Pageof 1
Sort By:
European Journal of Medical Genetics|February 16, 2010
Autosomal dominant microtiaS Chafai Elalaoui, I Cherkaoui Jaouad, L Rifai, et al.
Annals of Human Biology|October 14, 2010
Prevalence of MYH-associated polyposis related to three recurrent mutations in MoroccoF Z Laarabi, I Cherkaoui Jaouad, A Benazzouz, et al.
Journal of Biosocial Science|May 13, 2009
Consanguineous marriages in Morocco and the consequence for the incidence of autosomal recessive disordersI Cherkaoui Jaouad, S Chafaï Elalaoui, A Sbiti, et al.
Indian Journal of Pediatrics|November 18, 2008
Omenn syndrome with mutation in RAG1 geneI Cherkaoui Jaouad, K Ouldim, S Ali Ou Alla, et al.
European Journal of Medical Genetics|May 29, 2013
Inhabitual autosomal recessive form of dentin dysplasia type I in a large consanguineous Moroccan familyI Cherkaoui Jaouad, M El Alloussi, F Z Laarabi, et al.
Gene|January 24, 2012
The first mutations in the MYH gene reported in Moroccan colon cancer patientsF Z Laarabi, I Cherkaoui Jaouad, S Baert-Desurmont, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
European Journal of Medical Genetics|February 16, 2010
Autosomal dominant microtiaS Chafai Elalaoui, I Cherkaoui Jaouad, L Rifai, et al.
Annals of Human Biology|October 14, 2010
Prevalence of MYH-associated polyposis related to three recurrent mutations in MoroccoF Z Laarabi, I Cherkaoui Jaouad, A Benazzouz, et al.
Journal of Biosocial Science|May 13, 2009
Consanguineous marriages in Morocco and the consequence for the incidence of autosomal recessive disordersI Cherkaoui Jaouad, S Chafaï Elalaoui, A Sbiti, et al.
Indian Journal of Pediatrics|November 18, 2008
Omenn syndrome with mutation in RAG1 geneI Cherkaoui Jaouad, K Ouldim, S Ali Ou Alla, et al.
European Journal of Medical Genetics|May 29, 2013
Inhabitual autosomal recessive form of dentin dysplasia type I in a large consanguineous Moroccan familyI Cherkaoui Jaouad, M El Alloussi, F Z Laarabi, et al.
Gene|January 24, 2012
The first mutations in the MYH gene reported in Moroccan colon cancer patientsF Z Laarabi, I Cherkaoui Jaouad, S Baert-Desurmont, et al.
Pageof 1