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Manu Jamwal

Showing results (31-40 of 63) with videos related to

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The Journal of Molecular Diagnostics : JMD|February 10, 2020
Next-Generation Sequencing-Based Diagnosis of Unexplained Inherited Hemolytic Anemias Reveals Wide Genetic and Phenotypic HeterogeneityManu Jamwal, Anu Aggarwal, Arindam Palodhi, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 27, 2022
Prenatal diagnosis for hemophilia A (intron 22 inversion) reveals a rare association with Klinefelter syndrome with diagnostic difficulties in molecular interpretationRitika Sharma, Manu Jamwal, Harikishan Senee, et al.
Leukemia & Lymphoma|April 17, 2019
A novel germline <i>RUNX1</i> mutation with co-occurrence of somatic alterations in a case of myeloid neoplasm with familial thrombocytopenia: first report from IndiaSweta Rajpal, Arihant Jain, Manu Jamwal, et al.
The Journal of Molecular Diagnostics : JMD|February 24, 2018
Optimal Reference Gene Selection for Expression Studies in Human ReticulocytesAnu Aggarwal, Manu Jamwal, Ganesh K Viswanathan, et al.
Pathology|November 6, 2017
First report of Mediterranean stomatocytosis/macrothrombocytopenia in an Indian family: a diagnostic dilemmaManu Jamwal, Anu Aggarwal, Arindam Maitra, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 31, 2026
Combining conventional and reticulocyte metrics enhances Iron deficiency detection in asymptomatic individualsMugdha Gautam, Prashant Sharma, Arnab Pal, et al.
Hemoglobin|February 11, 2022
Hb Mizuho (<i>HBB</i>: c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation SequencingDiksha D Yadav, Manu Jamwal, Namrata Singh, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 12, 2024
Unearthing the genotype-inhibitor phenotype association in severe haemophilia A: A north Indian cohort studyDebadrita Ray, Ritika Sharma, Narender Kumar, et al.
Pediatric Blood & Cancer|June 12, 2021
Familial genotypic and phenotypic heterogeneity and its implications on genetic counseling exemplified in two cases of hereditary pyropoikilocytosis/erythrocytic spectrin-linked hemolytic anemia masquerading as congenital dyserythropoietic anemiaManu Jamwal, Anu Aggarwal, Prashant Sharma, et al.
Journal of Clinical Pathology|December 20, 2023
Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfallManu Jamwal, Sreejesh Sreedharanunni, Ravina Taak, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
The Journal of Molecular Diagnostics : JMD|February 10, 2020
Next-Generation Sequencing-Based Diagnosis of Unexplained Inherited Hemolytic Anemias Reveals Wide Genetic and Phenotypic HeterogeneityManu Jamwal, Anu Aggarwal, Arindam Palodhi, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 27, 2022
Prenatal diagnosis for hemophilia A (intron 22 inversion) reveals a rare association with Klinefelter syndrome with diagnostic difficulties in molecular interpretationRitika Sharma, Manu Jamwal, Harikishan Senee, et al.
Leukemia & Lymphoma|April 17, 2019
A novel germline <i>RUNX1</i> mutation with co-occurrence of somatic alterations in a case of myeloid neoplasm with familial thrombocytopenia: first report from IndiaSweta Rajpal, Arihant Jain, Manu Jamwal, et al.
The Journal of Molecular Diagnostics : JMD|February 24, 2018
Optimal Reference Gene Selection for Expression Studies in Human ReticulocytesAnu Aggarwal, Manu Jamwal, Ganesh K Viswanathan, et al.
Pathology|November 6, 2017
First report of Mediterranean stomatocytosis/macrothrombocytopenia in an Indian family: a diagnostic dilemmaManu Jamwal, Anu Aggarwal, Arindam Maitra, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 31, 2026
Combining conventional and reticulocyte metrics enhances Iron deficiency detection in asymptomatic individualsMugdha Gautam, Prashant Sharma, Arnab Pal, et al.
Hemoglobin|February 11, 2022
Hb Mizuho (<i>HBB</i>: c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation SequencingDiksha D Yadav, Manu Jamwal, Namrata Singh, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 12, 2024
Unearthing the genotype-inhibitor phenotype association in severe haemophilia A: A north Indian cohort studyDebadrita Ray, Ritika Sharma, Narender Kumar, et al.
Pediatric Blood & Cancer|June 12, 2021
Familial genotypic and phenotypic heterogeneity and its implications on genetic counseling exemplified in two cases of hereditary pyropoikilocytosis/erythrocytic spectrin-linked hemolytic anemia masquerading as congenital dyserythropoietic anemiaManu Jamwal, Anu Aggarwal, Prashant Sharma, et al.
Journal of Clinical Pathology|December 20, 2023
Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfallManu Jamwal, Sreejesh Sreedharanunni, Ravina Taak, et al.
Pageof 7