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Glucose-6-phosphate dehydrogenase (G6PD) deficiency, abnormal haemoglobins, and thalassaemia in Yugoslavia.

作者信息

Fraser G R, Grunwald P, Stamatoyannopoulos G

出版信息

J Med Genet. 1966 Mar;3(1):35-41. doi: 10.1136/jmg.3.1.35.

DOI:10.1136/jmg.3.1.35
PMID:5296509
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1012891/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4b7/1012891/f986bc179314/jmedgene00326-0040-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4b7/1012891/f986bc179314/jmedgene00326-0040-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4b7/1012891/f986bc179314/jmedgene00326-0040-a.jpg

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Am J Hum Genet. 1966 May;18(3):296-308.
3
G6PD deficiency in two autochthonous Croatian families.两个克罗地亚本地家庭中的葡萄糖-6-磷酸脱氢酶缺乏症

本文引用的文献

1
[On a case of association of thalassemia and "hereditary persistence of fetal hemoglobin"].[关于一例地中海贫血与“胎儿血红蛋白遗传性持续存在”的关联病例]
Haematologica. 1962;47:353-66.
2
Types of thalassaemia-trait carriers as revealed by a study of their incidence in Greece.通过对希腊地中海贫血特征携带者发病率的研究揭示的携带者类型。
Br J Haematol. 1962 Jan;8:5-14. doi: 10.1111/j.1365-2141.1962.tb06489.x.
3
HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN IN GREECE. A STUDY AND A COMPARISON.希腊胎儿血红蛋白的遗传性持续存在。一项研究与比较。
J Med Genet. 1969 Sep;6(3):281-5. doi: 10.1136/jmg.6.3.281.
4
Haemoglobin Lepore in Cyprus.塞浦路斯的血红蛋白Lepore
J Med Genet. 1975 Sep;12(3):275-9. doi: 10.1136/jmg.12.3.275.
Blood. 1964 Sep;24:223-40.
4
MILD GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN GREEK MALES.希腊男性中的轻度葡萄糖-6-磷酸脱氢酶缺乏症
Lancet. 1964 Oct 31;2(7366):932-5. doi: 10.1016/s0140-6736(64)90863-3.
5
A THALASSAEMIC TRAIT IN GIPSIES?吉普赛人中的地中海贫血特质？
Acta Med Scand. 1963 Sep;174:261-3. doi: 10.1111/j.0954-6820.1963.tb07921.x.
6
Genetical linkage between the loci for glucose-6-phosphate dehydrogenase deficiency and colour-blindness in American Negroes.美国黑人中葡萄糖-6-磷酸脱氢酶缺乏症基因座与色盲基因座之间的遗传连锁
Ann Hum Genet. 1962 Nov;26:107-22. doi: 10.1111/j.1469-1809.1962.tb01316.x.
7
[A case of thalassemia minor].[一例轻型地中海贫血病例]
Lijec Vjesn. 1962 Jul;84:673-8.
8
A new hereditary hemoglobinopathy (the Lepore trait) and its interaction with thalassemia trait.一种新的遗传性血红蛋白病（Lepore性状）及其与地中海贫血性状的相互作用。
Blood. 1958 Sep;13(9):835-44.
9
[A case of erythroblastic hemolytic anemia of Cooley's type].[一例库利氏型幼红细胞性溶血性贫血病例]
Srp Arh Celok Lek. 1952 Dec;80(12):1178-81.