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Sona Nair

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

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Haematologica|December 14, 2004
A novel Ser123Pro substitution in the MIDAS domain of integrin 3 associated with variant Glanzmann's thrombasthenia in an Indian patientSona Nair, Kanjaksha Ghosh, Shrimati Shetty, et al.
Platelets|December 19, 2002
Glanzmann's thrombasthenia: updatedSona Nair, Kanjaksha Ghosh, Bipin Kulkarni, et al.
British Journal of Haematology|October 31, 2002
Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the diseaseKanjaksha Ghosh, Bipin Kulkarni, Sona Nair, 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.
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.
Hematology (Amsterdam, Netherlands)|October 1, 2013
Hb Koln [β98(FG5) [GTG → ATG, Val → Met]: the first report from IndiaPrashant Warang, Sona Nair, Anita Nadkarni, et al.
Indian Journal of Human Genetics|December 17, 2013
Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from IndiaRanjeet Singh Mashon, Sona Nair, Pratibha Sawant, et al.
Thrombosis and Haemostasis|September 28, 2002
Two new beta3 integrin mutations in Indian patients with Glanzmann thrombasthenia: localization of mutations affecting cysteine residues in integrin beta3Sona Nair, Jihong Li, W Beau Mitchell, et al.
Hemoglobin|February 12, 2009
Hematological and molecular analysis of novel and rare beta-thalassemia mutations in the Indian populationAnita Nadkarni, Ajit Gorakshakar, Reema Surve, et al.
Blood Cells, Molecules & Diseases|October 29, 2008
Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotypeKhushnooma Italia, Dipty Jain, Sushma Gattani, et al.
Pageof 1

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

Sort By:
Pageof 1
Haematologica|December 14, 2004
A novel Ser123Pro substitution in the MIDAS domain of integrin 3 associated with variant Glanzmann's thrombasthenia in an Indian patientSona Nair, Kanjaksha Ghosh, Shrimati Shetty, et al.
Platelets|December 19, 2002
Glanzmann's thrombasthenia: updatedSona Nair, Kanjaksha Ghosh, Bipin Kulkarni, et al.
British Journal of Haematology|October 31, 2002
Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the diseaseKanjaksha Ghosh, Bipin Kulkarni, Sona Nair, 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.
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.
Hematology (Amsterdam, Netherlands)|October 1, 2013
Hb Koln [β98(FG5) [GTG → ATG, Val → Met]: the first report from IndiaPrashant Warang, Sona Nair, Anita Nadkarni, et al.
Indian Journal of Human Genetics|December 17, 2013
Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from IndiaRanjeet Singh Mashon, Sona Nair, Pratibha Sawant, et al.
Thrombosis and Haemostasis|September 28, 2002
Two new beta3 integrin mutations in Indian patients with Glanzmann thrombasthenia: localization of mutations affecting cysteine residues in integrin beta3Sona Nair, Jihong Li, W Beau Mitchell, et al.
Hemoglobin|February 12, 2009
Hematological and molecular analysis of novel and rare beta-thalassemia mutations in the Indian populationAnita Nadkarni, Ajit Gorakshakar, Reema Surve, et al.
Blood Cells, Molecules & Diseases|October 29, 2008
Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotypeKhushnooma Italia, Dipty Jain, Sushma Gattani, et al.
Pageof 1