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。 - Suppr

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A new hereditary hemoglobinopathy (the Lepore trait) and its interaction with thalassemia trait.

作者信息

GERALD P S, DIAMOND L K

出版信息

Blood. 1958 Sep;13(9):835-44.

PMID:13572441

Abstract

摘要

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引用本文的文献

Thalassaemia.

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Tris buffer for differentiation between haemoglobins C and E and separation of haemoglobins S from F and 'lepore' from A.

J Clin Pathol. 1961 Mar;14(2):200-1. doi: 10.1136/jcp.14.2.200.

Bibliography of human genetics.

Am J Hum Genet. 1959 Jun;11(2 Part 1):208-14 contd.

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

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

[Hb Frankfurt: a new unstable haemoglobin. II. Attempts to elucidate the structural aberrations].

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