Molecular pathogenesis and clinical variability of homozygous β0-thalassemia in populations of Jammu region of J&K state (India)
Author:
Affiliation:
1. Department of ZoologyHuman Genetic Research Cum Counselling Center, University of Jammu, Jammu, J&K 180006, India
Publisher
Informa UK Limited
Subject
Hematology,Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/10245330600921956
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2. Heterogeneity in ?0 thalassemia from Algeria: Genetic, clinical and molecular studies
3. Genetic interactions in thalassemia intermedia: Analysis of β-Mutations, α-Genotype, γ-Promoters, and β-LCR hypersensitive sites 2 and 4 in Italian patients
4. THE TURNOVER OF HEMOGLOBINS A, F, AND A2 IN THE PERIPHERAL BLOOD OF THREE PATIENTS WITH THALASSEMIA*
5. Molecular analysis of beta zero-thalassemia intermedia in Sardinia
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1. α- and β-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh;Hemoglobin;2023-01-02
2. The molecular characterization of Beta globin gene in thalassemia patients reveals rare and a novel mutations in Pakistani population;European Journal of Medical Genetics;2016-08
3. Thalassemia Major and Intermedia in Jammu and Kashmir, India: A Regional Transfusion Centre Experience;Indian Journal of Hematology and Blood Transfusion;2013-10-22
4. The genetics of blood disorders: the hereditary hemoglobinopathies;Jornal de Pediatria;2008-09-12
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