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Hemoglobin|October 30, 2014
An intriguing high performance liquid chromatogram of a double heterozygosity for Hb Q-India/Hb D-PunjabRama Kumari Badyal, Sanjeev Chhabra, Prashant Sharma, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|June 23, 2026
First Report of <i>MYH9</i> E1841K Variant in an Indian Family: A Case of Familial Macrothrombocytopenia and Review of LiteratureRitika Sharma, Manu Jamwal, Reena Das, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 23, 2026
Overcoming the PROSP pseudogene challenge: accurate diagnosis of a novel PROS1 variant in a patient with dural venous sinus thrombosisVasant Kumar, Debadrita Ray, Manu Jamwal, et al.
American Journal of Medical Genetics. Part A|October 28, 2020
Clericuzio-type poikiloderma with neutropenia in a patient from IndiaAnuradha Bishnoi, Manu Jamwal, Reena Das, 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.
Hemoglobin|August 21, 2015
β-Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β-Thalassemia is Rare in the Indian PopulationSreejesh Sreedharanunni, Sanjeev Chhabra, Jasbir Kaur Hira, 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.
International Journal of Medical Informatics|September 29, 2022
Performance analysis of machine learning algorithms and screening formulae for β-thalassemia trait screening of Indian antenatal womenReena Das, Sarkaft Saleh, Izabela Nielsen, et al.
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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 2, 2015
Hb M-Iwate in an Indian familyGanesh V Kumar, Prashant Sharma, Sanjeev Chhabra, et al.
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