一个苏丹家庭中的镰状细胞血红蛋白O病 - Suppr

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超能文献

Sickle-cell haemoglobin O disease in a Sudanese family.

作者信息

Ibrahim S A, Mustafa D

出版信息

Br Med J. 1967 Sep 16;3(5567):715-7. doi: 10.1136/bmj.3.5567.715.

DOI:10.1136/bmj.3.5567.715

PMID:6038366

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1843069/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a73/1843069/16c1627d458a/brmedj02153-0049-a.jpg

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本文引用的文献

A Third Abnormal Hemoglobin Associated with Hereditary Hemolytic Anemia.一种与遗传性溶血性贫血相关的第三种异常血红蛋白。

Proc Natl Acad Sci U S A. 1951 Dec;37(12):775-84. doi: 10.1073/pnas.37.12.775.

A new inherited abnormality of human hemoglobin.一种新的人类血红蛋白遗传性异常。

Proc Natl Acad Sci U S A. 1950 Nov;36(11):613-7. doi: 10.1073/pnas.36.11.613.

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Agglutinating-sickling arterial thrombosis. An unusual case of sickle-cell haemoglobin-C-disease.

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East Afr Med J. 1962 May;39:213-21.

Chemical heterogeneity of haemoglobin O.血红蛋白O的化学异质性

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