Homozygous beta delta-thalassaemia. Description of a case and review of the literature.
作者信息
Tsistrakis G A, Amarantos S P, Konkouris L L
出版信息
Acta Haematol. 1974;51(3):185-91. doi: 10.1159/000208292.
PMID:4218433
Abstract
摘要
相似文献
1
Homozygous beta delta-thalassaemia. Description of a case and review of the literature.
Acta Haematol. 1974;51(3):185-91. doi: 10.1159/000208292.
2
A family with three beta-delta-thalassemia homozygotes.
Blood. 1970 Feb;35(2):158-65.
3
Two families with different expression of homozygous beta-thalassaemia.
Acta Haematol. 1969;41(2):114-20. doi: 10.1159/000208839.
4
Beta-thalassaemia in Cuba.
Haematologia (Budap). 1974;8(1-4):71-9.
5
[Homozygote beta-thalassemia (Cooley's anemia) in a German family].
Folia Haematol Int Mag Klin Morphol Blutforsch. 1969;92(2):205-14.
6
The silent carrier of beta thalassemia.
N Engl J Med. 1969 Dec 11;281(24):1327-33. doi: 10.1056/NEJM196912112812403.
7
Absence of haemoglobin A in an individual simultaneously heterozygous in the genes for hereditary persistence of foetal haemoglobin and beta-thalassemia.
Br J Haematol. 1974 Apr;26(4):527-33. doi: 10.1111/j.1365-2141.1974.tb00496.x.
8
THE IRON-BINDING CAPACITY OF THALASSEMIC INDIVIDUALS.
Acta Genet Med Gemellol (Roma). 1964 Oct;13:418-22. doi: 10.1017/s1120962300015523.
9
Various aspects of alpha-thalassemia.
Ann N Y Acad Sci. 1974;232(0):152-8. doi: 10.1111/j.1749-6632.1974.tb20580.x.
10
Gamma-beta thalassemia: a cause of hemolytic disease of the newborn.
N Engl J Med. 1972 Jan 20;286(3):129-34. doi: 10.1056/NEJM197201202860304.
Zotero 插件