Sickle-cell-thalassaemia disease in South Turkey.
作者信息
AKSOY M, LEHMANN H
出版信息
Br Med J. 1957 Mar 30;1(5021):734-8. doi: 10.1136/bmj.1.5021.734.
Abstract
摘要
相似文献
1
Sickle-cell-thalassaemia disease in South Turkey.土耳其南部的镰状细胞-地中海贫血病
Br Med J. 1957 Mar 30;1(5021):734-8. doi: 10.1136/bmj.1.5021.734.
2
Hb.S-thalassaemia disease in India.印度的血红蛋白S-地中海贫血病
J Indian Med Assoc. 1958 Jan 1;30(1):4-8.
3
The thalassaemia syndromes. VI. Two subtypes of sickle cell-beta thalassaemia disease: (a) normocytic type of sickle cell-beta thalassaemia disease (b) microcytic type of sickle cell-beta thalassaemia disease.地中海贫血综合征。VI. 镰状细胞-β地中海贫血病的两种亚型：(a) 镰状细胞-β地中海贫血病的正细胞型 (b) 镰状细胞-β地中海贫血病的小细胞型
Acta Haematol. 1967;37(4):181-8. doi: 10.1159/000209068.
4
Benign sickle cell-thalassemia disease and cryptic thalassemia in a Negro family.一个黑人家庭中的良性镰状细胞-地中海贫血病及隐匿性地中海贫血
Ann Intern Med. 1962 Jul;57:121-8. doi: 10.7326/0003-4819-57-1-121.
5
[Thalassemia and sickle-cell disease in Norway].[挪威的地中海贫血和镰状细胞病]
Tidsskr Nor Laegeforen. 2001 Feb 28;121(6):678-80.
6
Sickle-cell anaemia in adults and its differentiation from sickle-cell thalassaemia.成人镰状细胞贫血及其与镰状细胞地中海贫血的鉴别诊断。
Lancet. 1958 Oct 18;2(7051):824-6. doi: 10.1016/s0140-6736(58)90378-7.
7
Sickle cell haemoglobin and two types of thalassaemia in the same family.同一家庭中的镰状细胞血红蛋白和两种类型的地中海贫血。
Acta Haematol. 1962;28:329-40. doi: 10.1159/000207298.
8
[Clinical and morphological observations on a case of microdrepanocytosis].
Folia Hered Pathol (Milano). 1962 Apr;11:101-24.
9
[Thalasso-sickle cell anemia. I].[海洋性贫血-镰状细胞贫血。I]
Sem Hop. 1959 Jan 24;35(4/1):271-8/P.
10
[Silvestroni-Bianco thalasso-drepanocytosis. (Apropos of a case)].[西尔韦斯特罗尼-比安科海洋性贫血-镰状细胞贫血症。（关于一例病例）]
Bull Mens Soc Med Mil Fr. 1962 Jun;56:177-81.
引用本文的文献
1
2
Bibliography of human genetics.人类遗传学文献目录。
Am J Hum Genet. 1958 Jun;10(2):235-48.
3
The suppression of haemoglobin E synthesis when hemoglobin H disease and hemoglobin E trait occur together.血红蛋白H病与血红蛋白E性状同时出现时血红蛋白E合成的抑制。
Humangenetik. 1967;3(4):312-8. doi: 10.1007/BF00292281.
本文引用的文献
1
Sickle cell anemia a molecular disease.镰状细胞贫血是一种分子疾病。
Science. 1949 Nov 25;110(2865):543-8. doi: 10.1126/science.110.2865.543.
2
[Further research on genetics in sickle cell anemia].[镰状细胞贫血的遗传学进一步研究]
Pediatria (Napoli). 1951 Nov-Dec;59(11-12):789-98.
3
4
Chronic hemolytic anemia associated with thalassemia and sickling traits.与地中海贫血和镰状细胞性状相关的慢性溶血性贫血。
Blood. 1952 Mar;7(3):350-7.
5
Presence of Foetal Haemoglobin in Cooley's anaemia.胎儿血红蛋白在库利贫血中的存在情况。
Nature. 1951 Jun 9;167(4258):950-1. doi: 10.1038/167950b0.
6
7
8
9
Sickle-cell trait in South Turkey.
Lancet. 1955 Mar 19;268(6864):589-90. doi: 10.1016/s0140-6736(55)91636-6.
10
A family illustrating the double inheritance of the sickle cell trait and of Mediterranean anaemia.一个体现镰状细胞性状和地中海贫血双重遗传的家族。
J Clin Pathol. 1954 Aug;7(3):201-8. doi: 10.1136/jcp.7.3.201.
Zotero 插件