?*-thalassemia intermedia with low HbF
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Genetics(clinical),Drug Discovery,Molecular Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF01496661.pdf
Reference29 articles.
1. Aksoy M, Bermek E, Almis G, Kutlar A (1982) ?-Thalassemia intermedia homozygous for normal hemoglobin A2 ?-thalassemia. Study of four families. Acta Haematol (Basel) 67:57?61
2. Aksoy M, Dinçol G, Erdem S (1978) Different types of beta-thalassemia intermedia. A genetic study in 20 patients. Acta Haematol (Basel) 59:178?189
3. Beaven GH, Ellis MJ, White JC (1961) Studies on human foetal haemoglobin. II. The hereditary haemoglobinopathies and thalassaemias. Br J Haematol 7:169?186
4. Bianco I, Graziani B, Carboni C (1977) Genetic patterns in thalassemia intermedia (constitutional microcytic anemia). Familial, hematologic and biosynthetic studies. Hum Hered 27:257?272
5. Brancati C, Baglioni C (1966) Homozygous ??-thalassaemia (?? microcythaemia). Nature 212:262?264
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Relationship of the Interaction Between Two Quantitative Trait Loci with γ-Globin Expression in β-Thalassemia Intermedia Patients;Hemoglobin;2018-03-04
2. Clinical and haematological evaluation of beta thalassaemia intermedia characterised by unusually low Hb F and increased Hb A2: beta thalassaemia intermedia II.;Journal of Medical Genetics;1985-06-01
3. Hereditary haemoglobin disorders in Brazil;Transactions of the Royal Society of Tropical Medicine and Hygiene;1985-01
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