单个红细胞葡萄糖-6-磷酸脱氢酶活性的研究：用于鉴定葡萄糖-6-磷酸脱氢酶缺乏症杂合子女性的高铁血红蛋白洗脱试验。 - Suppr

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超能文献

Studies of Glucose-6-Phosphate Dehydrogenase Activity of Individual Erythrocytes: The Methemoglobin-Elution Test for Identification of Females Heterozygous for G6PD Deficiency.

作者信息

Gall J C, Brewer G J, Dern R J

出版信息

Am J Hum Genet. 1965 Jul;17(4):359-68.

PMID:17948502

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1932613/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b03/1932613/c99d887767a8/ajhg00544-0075-a.jpg

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[DEMONSTRATION ON BLOOD SMEARS OF A DOUBLE ERYTHROCYTE POPULATION IN WOMEN HETEROZYGOUS FOR GLUCOSE-6-P DEHYDROGENASE DEFICIENCY].

Pathologica. 1963 Sep-Oct;55:371-5.

THE SEPARATION OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE-DEFICIENT ERYTHROCYTES FROM THE BLOOD OF HETEROZYGOTES FOR GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY.

Lancet. 1964 Jan 25;1(7326):189-92. doi: 10.1016/s0140-6736(64)92286-x.

METHEMOGLOBIN REDUCTION. STUDIES OF THE INTERACTION BETWEEN CELL POPULATIONS AND OF THE ROLE OF METHYLENE BLUE.

Blood. 1963 Sep;22:323-33.

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Arch Intern Med. 1962 Feb;109:209-34. doi: 10.1001/archinte.1962.03620140081013.

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