β-Cluster Haplotypes, α-Gene Status, and Hematological Data from SS, SC, and S-β-Thalassemia Patients in Southern California-Reference-Cited by-同舟云学术

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β-Cluster Haplotypes, α-Gene Status, and Hematological Data from SS, SC, and S-β-Thalassemia Patients in Southern California

Published:1989-01 Issue:4 Volume:13 Page:325-353
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Schroeder W. A.,Powars Darleen R.,Kay Lois M.,Chan Linda S.,Huynh Van,Shelton Joan B.,Shelton J. Roger

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630268909003397

Reference56 articles.

1. Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation.

2. Quantitative microchromatographic determination of hemoglobin f in patients with hemoglobins s and/or c

3. Microchromatography of hemoglobins

4. Microchromatography of hemoglobins

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4. Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyurea;Blood Advances;2018-03-19

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