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

Roshan B Colah

Showing results (31-40 of 86) with videos related to

Pageof 9
Sort By:
Annals of Human Biology|June 10, 2010
Restriction fragment length polymorphism (RFLP) of the X chromosome linked glucose-6-phosphate dehydrogenase (G6PD) locus in IndiaRati Chalvam, Roshan B Colah, Dipika Mohanty, et al.
Genetic Testing and Molecular Biomarkers|January 5, 2011
Association of (GT)n repeats promoter polymorphism of heme oxygenase-1 gene with serum bilirubin levels in healthy Indian adultsSelma D'Silva, Vikrant Borse, Roshan B Colah, et al.
Hematology (Amsterdam, Netherlands)|March 14, 2014
Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patientsPooja S Dabke, Roshan B Colah, Kanjaksha K Ghosh, et al.
Blood Cells, Molecules & Diseases|June 30, 2009
Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency among the tribals in Western IndiaRati Chalvam, Roshan B Colah, Dipika Mohanty, et al.
Hemoglobin|November 9, 2013
Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in CisStacy Colaco, Amee Trivedi, Roshan B Colah, et al.
Journal of Child Neurology|January 14, 2014
Neurometabolic disorder with microcephaly, dystonia, and central cyanosis masquerading as cerebral palsyKalpana Devadathan, Mini Sreedharan, Sanuja Sarasam, et al.
Hemoglobin|June 5, 2003
Co-existence of the codon 16 (-C) (beta(o)) and codon 10 (C --> A) (beta+) mutations on the same beta-globin geneRoshan B Colah, Anita Nadkarni, Aruna Pawar, et al.
Mediterranean Journal of Hematology and Infectious Diseases|July 22, 2014
A Case of Iron Deficiency Anemia with Co-existing Hb FontainebleauAbhishek Purohit, Mukul Aggarwal, Roshan B Colah, et al.
Hemoglobin|September 15, 2016
Hb E-β-Thalassemia in Five Indian StatesKhushnooma Italia, Pooja Dabke, Pratibha Sawant, et al.
Blood Cells, Molecules & Diseases|October 30, 2007
A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemiaPrabhakar S Kedar, Prashant Warang, Anita H Nadkarni, et al.
Pageof 9

Showing results (31-40 of 86) with videos related to

Sort By:
Pageof 9
Annals of Human Biology|June 10, 2010
Restriction fragment length polymorphism (RFLP) of the X chromosome linked glucose-6-phosphate dehydrogenase (G6PD) locus in IndiaRati Chalvam, Roshan B Colah, Dipika Mohanty, et al.
Genetic Testing and Molecular Biomarkers|January 5, 2011
Association of (GT)n repeats promoter polymorphism of heme oxygenase-1 gene with serum bilirubin levels in healthy Indian adultsSelma D'Silva, Vikrant Borse, Roshan B Colah, et al.
Hematology (Amsterdam, Netherlands)|March 14, 2014
Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patientsPooja S Dabke, Roshan B Colah, Kanjaksha K Ghosh, et al.
Blood Cells, Molecules & Diseases|June 30, 2009
Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency among the tribals in Western IndiaRati Chalvam, Roshan B Colah, Dipika Mohanty, et al.
Hemoglobin|November 9, 2013
Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in CisStacy Colaco, Amee Trivedi, Roshan B Colah, et al.
Journal of Child Neurology|January 14, 2014
Neurometabolic disorder with microcephaly, dystonia, and central cyanosis masquerading as cerebral palsyKalpana Devadathan, Mini Sreedharan, Sanuja Sarasam, et al.
Hemoglobin|June 5, 2003
Co-existence of the codon 16 (-C) (beta(o)) and codon 10 (C --> A) (beta+) mutations on the same beta-globin geneRoshan B Colah, Anita Nadkarni, Aruna Pawar, et al.
Mediterranean Journal of Hematology and Infectious Diseases|July 22, 2014
A Case of Iron Deficiency Anemia with Co-existing Hb FontainebleauAbhishek Purohit, Mukul Aggarwal, Roshan B Colah, et al.
Hemoglobin|September 15, 2016
Hb E-β-Thalassemia in Five Indian StatesKhushnooma Italia, Pooja Dabke, Pratibha Sawant, et al.
Blood Cells, Molecules & Diseases|October 30, 2007
A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemiaPrabhakar S Kedar, Prashant Warang, Anita H Nadkarni, et al.
Pageof 9