Thalassemia intermedia in two patients with Hb lepore-β°-thalassemia (Frameshift codon 8, -AA)
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269409043627
Reference18 articles.
1. A New Hereditary Hemoglobinopathy (the Lepore Trait) and Its Interaction with Thalassemia Trait
2. Abnormal human hemoglobins X. A study of hemoglobin leporeBoston
3. Hemoglobins Lepore and Anti-Lepore
4. Hb Lepore-Hb C and Hb Lepore-β°-Thalassemia Compound Heterozygotes1 N an Algerian Family
5. Identification of HB Lepore-Mashington-Boston in Association with HB E [βB26(B8)GLU→LYS] in a Thai Female
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1. First Observation of Hb Lepore Hollandia in the Baiga Tribal Family;Indian Journal of Hematology and Blood Transfusion;2018-02-27
2. Association of Hb S/Hb lepore and δβ-thalassemia/Hb lepore in Sicilian patients: Review of the presence of Hb lepore in Sicily;European Journal of Haematology;2009-04-24
3. Hb Lepore in the Indian Population;Hemoglobin;2003-01
4. FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999);Hemoglobin;2001-01
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