α地中海贫血：三个华裔加拿大家庭中的5例血红蛋白H病 - Suppr

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超能文献

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/8b12/1924320/0f4229ec5098/canmedaj01274-0013-a.jpg

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本文引用的文献

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.

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.

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.

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.

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.

HUMAN HAEMOGLOBINS.人类血红蛋白

J Med Genet. 1965 Mar;2(1):48-90. doi: 10.1136/jmg.2.1.48.

THE IN VITRO SYNTHESIS OF HEMOGLOBIN BY HUMAN BONE MARROW IN THALASSEMIA.

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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.

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.

HAEMOGLOBIN BART'S AND H IN A SWEDISH BOY.

Acta Haematol. 1964 Oct;32:239-49. doi: 10.1159/000209592.

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