Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous Hb-C disease, SC disease, and various combinations of hemoglobin variants.

Clinica chimica acta; international journal of clinical chemistry ·Vol. 38 ·No. 1 ·1972-04-00 ·Pages 5-16

Huisman TH, Schroeder WA, Bouver NG, Miller A, Shelton JR, Shelton JB, Apell G

Abstract

暂无摘要

MeSH Terms

Adolescent Adult Aged Aging Alanine/analysis Anemia, Sickle Cell/blood Child Child, Preschool Chromatography, Ion Exchange Electrophoresis, Starch Gel Female Fetal Hemoglobin/analysis,metabolism Glycine/analysis Hemoglobin C Disease/blood Hemoglobinopathies/blood Hemoglobins, Abnormal/analysis Heterozygote Homozygote Humans Infant Macromolecular Substances Male Middle Aged Sex Factors

Chemicals

Hemoglobins, Abnormal Macromolecular Substances Fetal Hemoglobin Alanine Glycine

Authors & Affiliations

7 authors, click to expand affiliations / ORCID

Huisman T H

Schroeder W A

Bouver N G

Miller A

Shelton J R

Shelton J B

Apell G

Article Info

Journal

Clinica chimica acta; international journal of clinical chemistry

Abbr.

Clin Chim Acta

ISSN

0009-8981

DOI

10.1016/0009-8981(72)90201-x

Published

1972-04-00

Pages

5-16

Language

English

Region

Netherlands

NLM ID

1302422

Subset

External Links

PubMed source DOI: 10.1016/0009-8981(72)90201-x View journal details

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Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous Hb-C disease, SC disease, and various combinations of hemoglobin variants.

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