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

O Dunda

Showing results (11-20 of 14) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 14 results.
Blood|April 1, 1987
The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF levelR L Nagel, S K Rao, O Dunda-Belkhodja, et al.
Nouvelle Revue Francaise D'Hematologie|October 1, 1994
Fetal haemoglobin variations following hydroxyurea treatment in patients with cyanotic congenital heart diseaseP Triadou, M Maier-Redelsperger, R Krishnamoorty, et al.
Human Genetics|May 1, 1992
A novel sickle cell mutation of yet another origin in Africa: the Cameroon typeC Lapouméroulie, O Dunda, R Ducrocq, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1985
Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patientsD Labie, J Pagnier, C Lapoumeroulie, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Blood|April 1, 1987
The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF levelR L Nagel, S K Rao, O Dunda-Belkhodja, et al.
Nouvelle Revue Francaise D'Hematologie|October 1, 1994
Fetal haemoglobin variations following hydroxyurea treatment in patients with cyanotic congenital heart diseaseP Triadou, M Maier-Redelsperger, R Krishnamoorty, et al.
Human Genetics|May 1, 1992
A novel sickle cell mutation of yet another origin in Africa: the Cameroon typeC Lapouméroulie, O Dunda, R Ducrocq, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1985
Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patientsD Labie, J Pagnier, C Lapoumeroulie, et al.
Pageof 2