一个拥有血红蛋白S和C以及典型地中海贫血的家族的遗传学研究。 - Suppr

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Genetic Study of a Family Possessing Hemoglobins S and C, and Classical Thalassemia.

作者信息

McCurdy P R, Pearson H A

出版信息

Am J Hum Genet. 1961 Dec;13(4):390-5.

PMID:17948459

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1932131/

Abstract

摘要

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引用本文的文献

HUMAN HEMOGLOBIN GENE LINKAGE: REPORT OF A FAMILY WITH HEMOGLOBIN B2, HEMOGLOBIN S, AND BETA THALASSEMIA, INCLUDING A PROBABLE CROSSOVER BETWEEN THALASSEMIA AND DELTA LOCI.

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本文引用的文献

Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

Blood. 1951 May;6(5):413-28.

Genetic basis of the thalassaemia diseases.

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Identity of haemoglobin A2.

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Starch block electrophoresis of hemoglobin.

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Br J Haematol. 1959 Jan;5(1):102-20. doi: 10.1111/j.1365-2141.1959.tb04016.x.

Allelomorphism and the chemical differences of the human haemoglobins A, S and C.

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Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin.

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Qualitative and quantitative control of adult hemoglobin synthesis; a multiple allele hypothesis.

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