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Roshan B Colah

Showing results (21-30 of 86) with videos related to

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The Indian Journal of Medical Research|July 4, 2015
Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India - Country scenarioMalay B Mukherjee, Roshan B Colah, Snehal Martin, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|May 29, 2002
Chronic persistent hemolysis in an infant: can we afford to forget malaria as a cause?Prabhakar S Kedar, Kanjaksha Ghosh, Roshan B Colah, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|November 30, 2011
G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in IndiaSelma D'Silva, Roshan B Colah, Kanjaksha Ghosh, et al.
The Indian Journal of Medical Research|July 4, 2015
Sickle cell disease in tribal populations in IndiaRoshan B Colah, Malay B Mukherjee, Snehal Martin, et al.
Blood Cells, Molecules & Diseases|July 6, 2005
Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G-->A mutationSridevi Sukumar, Malay B Mukherjee, Roshan B Colah, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 20, 2004
Hereditary spherocytosis in association with severe G6PD deficiency: report of an unusual casePrabhakar S Kedar, Roshan B Colah, Kanjaksha Ghosh, et al.
International Journal of Laboratory Hematology|March 20, 2024
Wide spectrum of novel and rare hemoglobin variants in the multi-ethnic Indian population: A reviewPallavi Thaker, Namrata Mahajan, Malay B Mukherjee, et al.
Hemoglobin|February 2, 2010
Hb H disease due to homozygosity for a rare alpha2-globin variant, Hb SallanchesPrashant Warang, Sona Nair, Anita Nadkarni, et al.
Hemoglobin|March 23, 2013
Variable presentation of HB H disease due to homozygosity for the rare polyadenylation signal A T(Indian) (AATAAA>AATA- -) mutation in four Indian familiesSona B Nair, Anita H Nadkarni, Kanjaksha Ghosh, et al.
Indian Journal of Human Genetics|July 4, 2012
SRY sequence in maternal plasma: Implications for non-invasive prenatal diagnosis: First report from IndiaEdna D'Souza, Sona Nair, Anita Nadkarni, et al.
Pageof 9

Showing results (21-30 of 86) with videos related to

Sort By:
Pageof 9
The Indian Journal of Medical Research|July 4, 2015
Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India - Country scenarioMalay B Mukherjee, Roshan B Colah, Snehal Martin, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|May 29, 2002
Chronic persistent hemolysis in an infant: can we afford to forget malaria as a cause?Prabhakar S Kedar, Kanjaksha Ghosh, Roshan B Colah, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|November 30, 2011
G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in IndiaSelma D'Silva, Roshan B Colah, Kanjaksha Ghosh, et al.
The Indian Journal of Medical Research|July 4, 2015
Sickle cell disease in tribal populations in IndiaRoshan B Colah, Malay B Mukherjee, Snehal Martin, et al.
Blood Cells, Molecules & Diseases|July 6, 2005
Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G-->A mutationSridevi Sukumar, Malay B Mukherjee, Roshan B Colah, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 20, 2004
Hereditary spherocytosis in association with severe G6PD deficiency: report of an unusual casePrabhakar S Kedar, Roshan B Colah, Kanjaksha Ghosh, et al.
International Journal of Laboratory Hematology|March 20, 2024
Wide spectrum of novel and rare hemoglobin variants in the multi-ethnic Indian population: A reviewPallavi Thaker, Namrata Mahajan, Malay B Mukherjee, et al.
Hemoglobin|February 2, 2010
Hb H disease due to homozygosity for a rare alpha2-globin variant, Hb SallanchesPrashant Warang, Sona Nair, Anita Nadkarni, et al.
Hemoglobin|March 23, 2013
Variable presentation of HB H disease due to homozygosity for the rare polyadenylation signal A T(Indian) (AATAAA>AATA- -) mutation in four Indian familiesSona B Nair, Anita H Nadkarni, Kanjaksha Ghosh, et al.
Indian Journal of Human Genetics|July 4, 2012
SRY sequence in maternal plasma: Implications for non-invasive prenatal diagnosis: First report from IndiaEdna D'Souza, Sona Nair, Anita Nadkarni, et al.
Pageof 9