THALASSEMIA INTERMEDIA: HETEROZYGOUSβ-THALASSEMIA AND CO-INHERITANCE OF ANαGENE TRIPLICATION
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1081/HEM-120015038
Reference4 articles.
1. Different hematological phenotypes caused by the interaction of triplicated α-globin genes and heterozygous β-thalassemia
2. Correspondence
3. The molecular basis of β thalassaemia in Punjabi and Maharashtran Indians includes a multilocus aetiology involving triplicated α-globin loci
4. Geographic and Ethnic Distribution of β-Thalassemia Mutations in Uttar Pradesh, India
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1. Hematological and genetic profiles of persons with co‐inherited heterozygous β‐thalassemia and supernumerary α‐globin genes;European Journal of Haematology;2023-01-14
2. Alpha‐globin gene triplication and its effect in beta‐thalassemia carrier, sickle cell trait, and healthy individual;eJHaem;2021-07-19
3. Interaction of anα-Globin Gene Triplication withβ-Globin Gene Mutations in Iranian Patients withβ-Thalassemia Intermedia;Hemoglobin;2015-05-04
4. Sickle Cell Anemia—Molecular Diagnosis and Prenatal Counseling: SGPGI Experience;The Indian Journal of Pediatrics;2011-06-29
5. Frequency of α-Globin Gene Triplications and Their Interaction with β-Thalassemia Mutations;Hemoglobin;2009-01
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