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

R B Colah

Showing results (1-10 of 36) with videos related to

Pageof 4
Sort By:
The Journal of the Association of Physicians of India|October 1, 1994
Strategies for prevention of thalassemia and hemoglobinopathiesR B Colah
Indian Journal of Medical Sciences|February 1, 1990
Community control of B-thalassemiaR B Colah
Blood|May 15, 1997
A novel beta+-thalassemia mutation (codon 10 GCC --> GCA) and a rare transcriptional mutation (-28A --> G) in IndiansA R Pawar, R B Colah, D Mohanty
The Indian Journal of Medical Research|November 7, 1998
Comparison of FPLC with cellulose acetate electrophoresis for the diagnosis of beta-thalassaemia traitS N Desai, R B Colah, D Mohanty
The Indian Journal of Medical Research|November 18, 2011
Invasive & non-invasive approaches for prenatal diagnosis of haemoglobinopathies: experiences from IndiaR B Colah, A C Gorakshakar, A H Nadkarni
American Journal of Hematology|January 30, 2003
G6PD deficiency and malaria in IndiaD Mohanty, S Sukumar, M B Mukherjee, et al.
American Journal of Hematology|June 8, 2001
A single mutation is responsible for the high prevalence of G6PD deficiency in the Vataliya Prajapatis--an endogamous caste group from Western IndiaS Sukumar, R B Colah, D Mohanty, et al.
Blood Cells, Molecules & Diseases|May 10, 2003
Molecular characterization of G6PD Insuli--a novel 989 CGC --> CAC (330 Arg --> His) mutation in the Indian populationS Sukumar, M B Mukherjee, R B Colah, et al.
American Journal of Hematology|November 14, 2000
Beta-thalassemia gene flow from India to MauritiusA C Gorakshakar, K Ghosh, R B Colah, et al.
American Journal of Hematology|October 1, 1996
Alpha genotyping in a heterogeneous Indian populationA H Nadkarni, A C Gorakshakar, D Mohanty, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
The Journal of the Association of Physicians of India|October 1, 1994
Strategies for prevention of thalassemia and hemoglobinopathiesR B Colah
Indian Journal of Medical Sciences|February 1, 1990
Community control of B-thalassemiaR B Colah
Blood|May 15, 1997
A novel beta+-thalassemia mutation (codon 10 GCC --> GCA) and a rare transcriptional mutation (-28A --> G) in IndiansA R Pawar, R B Colah, D Mohanty
The Indian Journal of Medical Research|November 7, 1998
Comparison of FPLC with cellulose acetate electrophoresis for the diagnosis of beta-thalassaemia traitS N Desai, R B Colah, D Mohanty
The Indian Journal of Medical Research|November 18, 2011
Invasive & non-invasive approaches for prenatal diagnosis of haemoglobinopathies: experiences from IndiaR B Colah, A C Gorakshakar, A H Nadkarni
American Journal of Hematology|January 30, 2003
G6PD deficiency and malaria in IndiaD Mohanty, S Sukumar, M B Mukherjee, et al.
American Journal of Hematology|June 8, 2001
A single mutation is responsible for the high prevalence of G6PD deficiency in the Vataliya Prajapatis--an endogamous caste group from Western IndiaS Sukumar, R B Colah, D Mohanty, et al.
Blood Cells, Molecules & Diseases|May 10, 2003
Molecular characterization of G6PD Insuli--a novel 989 CGC --> CAC (330 Arg --> His) mutation in the Indian populationS Sukumar, M B Mukherjee, R B Colah, et al.
American Journal of Hematology|November 14, 2000
Beta-thalassemia gene flow from India to MauritiusA C Gorakshakar, K Ghosh, R B Colah, et al.
American Journal of Hematology|October 1, 1996
Alpha genotyping in a heterogeneous Indian populationA H Nadkarni, A C Gorakshakar, D Mohanty, et al.
Pageof 4