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Alpha thalassemia: five cases of hemoglobin H disease in three Oriental-Canadian families.

作者信息

Ing R Y, Crookston J H

出版信息

Can Med Assoc J. 1968 Jul 13;99(2):49-56.

PMID:5664181
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1924320/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b12/1924320/d9c2639f0d71/canmedaj01274-0015-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b12/1924320/0f4229ec5098/canmedaj01274-0013-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b12/1924320/a3d5cb6c35de/canmedaj01274-0014-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b12/1924320/d9c2639f0d71/canmedaj01274-0015-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b12/1924320/0f4229ec5098/canmedaj01274-0013-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b12/1924320/a3d5cb6c35de/canmedaj01274-0014-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b12/1924320/d9c2639f0d71/canmedaj01274-0015-a.jpg

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[A2' (B2) hemoglobin associated with beta thalassemia and hereditary persistence of fetal hemoglobin. Study in 3 Colombian families].与β地中海贫血和胎儿血红蛋白遗传性持续存在相关的[A2'（B2）血红蛋白。对3个哥伦比亚家庭的研究]
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本文引用的文献

1
Thalassaemia and hydrops foetalis-family studies.地中海贫血和胎儿水肿——家族研究
Br Med J. 1967 Aug 5;3(5561):347-9. doi: 10.1136/bmj.3.5561.347.
2
Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.异常血红蛋白的研究。I. 通过碱变性法在镰状细胞贫血和其他血液系统疾病中的显示
Blood. 1951 May;6(5):413-28.
3
Inhomogeneity of hemoglobin. VI. The minor hemoglobin components of cord blood.血红蛋白的不均一性。VI. 脐血中的次要血红蛋白成分。
Blood. 1962 Sep;20:302-14.
4
Haemoglobin H disease with persistent haemoglobin "Bart's" in an Oriental Jewess and her daughter: a dual alpha-chain deficiency of human haemoglobin.一名东方犹太女性及其女儿患血红蛋白H病伴持续性血红蛋白“巴特氏”：人类血红蛋白的双α链缺乏症
Br Med J. 1959 Dec 5;2(5161):1228-30. doi: 10.1136/bmj.2.5161.1228.
5
HEMOGLOBIN ZUERICH; CLINICAL, CHEMICAL AND KINETIC STUDIES.血红蛋白苏黎世；临床、化学及动力学研究
Am J Med. 1965 Jul;39:4-20. doi: 10.1016/0002-9343(65)90241-x.
6
HUMAN HAEMOGLOBINS.人类血红蛋白
J Med Genet. 1965 Mar;2(1):48-90. doi: 10.1136/jmg.2.1.48.
7
THE IN VITRO SYNTHESIS OF HEMOGLOBIN BY HUMAN BONE MARROW IN THALASSEMIA.
Blood. 1965 Jun;25:897-906.
8
CURRENT CONCEPTS OF THE GENETICS OF THE THALASSEMIAS.地中海贫血遗传学的当前概念
Cold Spring Harb Symp Quant Biol. 1964;29:399-413. doi: 10.1101/sqb.1964.029.01.042.
9
THE METABOLISM OF THE INDIVIDUAL C14 LABELED HEMOGLOBINS IN PATIENTS WITH H-THALASSEMIA, WITH OBSERVATIONS ON RADIOCHROMATE BINDING TO THE HEMOGLOBINS DURING RED CELL SURVIVAL.H型地中海贫血患者中个体C14标记血红蛋白的代谢，以及红细胞存活期间放射性铬与血红蛋白结合情况的观察。
J Clin Invest. 1965 Feb;44(2):315-25. doi: 10.1172/JCI105145.
10
HAEMOGLOBIN BART'S AND H IN A SWEDISH BOY.
Acta Haematol. 1964 Oct;32:239-49. doi: 10.1159/000209592.