Elevated Hb F Associated with β-Thalassaemia Trait: Haemoglobin Synthesis in Reticulocytes and in Blood BFU-E-Reference-Cited by-同舟云学术

Elevated Hb F Associated with β-Thalassaemia Trait: Haemoglobin Synthesis in Reticulocytes and in Blood BFU-E

Published:2009-04-24 Issue:4 Volume:25 Page:339-346
ISSN:0036-553X
Container-title:Scandinavian Journal of Haematology
language:en
Short-container-title:

Author:

Dubart A.,Testa U.,Musumeci S.,Vainchenker W.,Beuzard Y.,Henri A.,Schirilo G.,Romeo M. A.,Russo G.,Rochant H.,Rosa J.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1981.tb01412.x/fullpdf

Reference32 articles.

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4. EVALUATION OF THE POOL OF α HEMOGLOBIN CHAINS AND STUDY OF THE DISSOCIATION OF THE HEMOGLOBIN MOLECULE INTO MONOMERS

5. Beta thalassemia and sickle cell disease in culture of early erythroid precursors: hemoglobin synthesis and ultrastructural study;Beuzard;Blood Cells,1980

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1. Understanding heterogeneity of fetal hemoglobin induction through comparative analysis of F and A erythroblasts;Blood;2020-05-28

2. Can a polymorphism in the thalassemia gene and a heterozygote CFTR mutation cause acute pancreatitis?;World Journal of Clinical Cases;2014

3. Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal ?-gene expression in association with ? thalassemia and linkage relationship with the ?-globin gene cluster;Human Genetics;1984-04

4. Unusual combination of genetic defects in a Sicilian boy: Gγ Aγ δβ thalassemia, Gγ Aγ heterocellular HPFH, βº thalassemia, and albinism;American Journal of Medical Genetics;1983-06

5. Genetic regulation of ? gene expression: Study of the interaction of ?-thalassemia with heterocellular HPFH;Human Genetics;1981-07