老挝血红蛋白疾病的高遗传多态性。由相关地中海贫血综合征导致的复杂表型。 - Suppr

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High genetic polymorphism of hemoglobin disorders in Laos. Complex phenotypes due to associated thalassemic syndromes.

作者信息

Sicard D, Lieurzou Y, Lapoumeroulie C, Labie D

出版信息

Hum Genet. 1979 Sep;50(3):327-36. doi: 10.1007/BF00399399.

DOI:10.1007/BF00399399

PMID:489017

Abstract

摘要

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High genetic polymorphism of hemoglobin disorders in Laos. Complex phenotypes due to associated thalassemic syndromes.老挝血红蛋白疾病的高遗传多态性。由相关地中海贫血综合征导致的复杂表型。

Hum Genet. 1979 Sep;50(3):327-36. doi: 10.1007/BF00399399.

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HEMOGLOBIN HOPE: A BETA CHAIN VARIANT.血红蛋白霍普：一种β链变体。

Blood. 1965 May;25:830-8.

THE COEXISTENCE OF THE GENES FOR HEMOGLOBIN E AND ALPHA-THALASSEMIA IN THAIS, WITH RESULTANT SUPPRESSION OF HEMOGLOBIN E SYNTHESIS.血红蛋白E基因与α地中海贫血基因在泰国人中的共存，导致血红蛋白E合成受到抑制。

Am J Hum Genet. 1964 Sep;16(3):311-35.

[FREQUENCY OF HEMOGLOBIN E IN LAOS].[老挝血红蛋白E的频率]

Med Trop (Mars). 1964 Jan-Feb;24:51-60.

Abnormal haemoglobins in the neonatal period and their relationship to thalassaemia.新生儿期的异常血红蛋白及其与地中海贫血的关系。

Br J Haematol. 1963 Jul;9:265-77. doi: 10.1111/j.1365-2141.1963.tb06551.x.

The suppression of haemoglobin E synthesis when hemoglobin H disease and hemoglobin E trait occur together.血红蛋白H病与血红蛋白E性状同时出现时血红蛋白E合成的抑制。

Humangenetik. 1967;3(4):312-8. doi: 10.1007/BF00292281.

Studies of the distribution of haemoglobin E, thalassaemias and glucose-6-phosphate dehydrogenase deficiency in north-eastern Thailand.

Nature. 1967 Apr 29;214(5087):501-2. doi: 10.1038/214501a0.

Abnormal human haemoglobins. Separation and characterization of the alpha and beta chains by chromatography, and the determination of two new variants, hb Chesapeak and hb J (Bangkok).异常人类血红蛋白。通过色谱法分离和鉴定α链和β链，并测定两种新变体，即血红蛋白切萨皮克和血红蛋白J（曼谷）。

J Mol Biol. 1966 Aug;19(1):91-108. doi: 10.1016/s0022-2836(66)80052-9.

Rapid electrophoresis and quantitation of haemoglobins on cellulose acetate.醋酸纤维素上血红蛋白的快速电泳及定量分析

J Clin Pathol. 1965 Nov;18(6):790-2. doi: 10.1136/jcp.18.6.790.

Fibrinogen Detroit--a molecular defect in the N-terminal disulphide knot of human fibrinogen?纤维蛋白原底特律——人类纤维蛋白原N端二硫键结中的分子缺陷？

Nature. 1968 Apr 13;218(5137):134-7. doi: 10.1038/218134a0.

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