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Manu Jamwal

Showing results (41-50 of 63) with videos related to

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Blood Cells, Molecules & Diseases|September 10, 2018
Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north IndiansBarjinderjit Kaur Dhillon, Gunjan Chopra, Manu Jamwal, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|May 6, 2024
Plasminogen Activator Inhibitor-1 4G/5G Promoter Polymorphism in Indian Patients with Deep Vein ThrombosisSaniya Sharma, Manu Jamwal, Varun Uppal, et al.
Journal of Cutaneous Pathology|February 4, 2022
Correlating clinical and laboratory diagnostic modalities in the diagnosis of epidermolysis bullosa in a resource-poor settingRahul Mahajan, Seema Manjunath, Manoj Gopal Madakshira, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|April 3, 2023
Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII DeficiencyRitika Sharma, Manu Jamwal, Namrata Singh, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|June 12, 2023
Correction to: Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII DeficiencyRitika Sharma, Manu Jamwal, Namrata Singh, et al.
The Journal of Molecular Diagnostics : JMD|February 15, 2024
Comprehensive Genomic Analysis Identifies a Diverse Landscape of Sideroblastic and Nonsideroblastic Iron-Related Anemias with Novel and Pathogenic Variants in an Iron-Deficient Endemic SettingPankaj Sharma, Prateek Bhatia, Minu Singh, et al.
Croatian Medical Journal|March 23, 2026
Correction to: Non-invasive prenatal testing of beta-hemoglobinopathies using next generation sequencing, in-silico sequence size selection, and haplotypingHenry A Erlich, Lily Ko, Jiyae Lee, et al.
Croatian Medical Journal|June 13, 2024
Non-invasive prenatal testing of beta-hemoglobinopathies using next generation sequencing, in-silico sequence size selection, and haplotypingHenry A Erlich, Lily Ko, Jiyae Lee, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 26, 2022
Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effectRitika Sharma, Manu Jamwal, Hari Kishan Senee, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|July 16, 2021
Next-Generation Sequencing Based Approach to Identify Underlying Genetic Defects of Glanzmann ThrombastheniaRitika Sharma, Manu Jamwal, Hari Kishan Senee, et al.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
Blood Cells, Molecules & Diseases|September 10, 2018
Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north IndiansBarjinderjit Kaur Dhillon, Gunjan Chopra, Manu Jamwal, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|May 6, 2024
Plasminogen Activator Inhibitor-1 4G/5G Promoter Polymorphism in Indian Patients with Deep Vein ThrombosisSaniya Sharma, Manu Jamwal, Varun Uppal, et al.
Journal of Cutaneous Pathology|February 4, 2022
Correlating clinical and laboratory diagnostic modalities in the diagnosis of epidermolysis bullosa in a resource-poor settingRahul Mahajan, Seema Manjunath, Manoj Gopal Madakshira, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|April 3, 2023
Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII DeficiencyRitika Sharma, Manu Jamwal, Namrata Singh, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|June 12, 2023
Correction to: Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII DeficiencyRitika Sharma, Manu Jamwal, Namrata Singh, et al.
The Journal of Molecular Diagnostics : JMD|February 15, 2024
Comprehensive Genomic Analysis Identifies a Diverse Landscape of Sideroblastic and Nonsideroblastic Iron-Related Anemias with Novel and Pathogenic Variants in an Iron-Deficient Endemic SettingPankaj Sharma, Prateek Bhatia, Minu Singh, et al.
Croatian Medical Journal|March 23, 2026
Correction to: Non-invasive prenatal testing of beta-hemoglobinopathies using next generation sequencing, in-silico sequence size selection, and haplotypingHenry A Erlich, Lily Ko, Jiyae Lee, et al.
Croatian Medical Journal|June 13, 2024
Non-invasive prenatal testing of beta-hemoglobinopathies using next generation sequencing, in-silico sequence size selection, and haplotypingHenry A Erlich, Lily Ko, Jiyae Lee, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 26, 2022
Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effectRitika Sharma, Manu Jamwal, Hari Kishan Senee, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|July 16, 2021
Next-Generation Sequencing Based Approach to Identify Underlying Genetic Defects of Glanzmann ThrombastheniaRitika Sharma, Manu Jamwal, Hari Kishan Senee, et al.
Pageof 7