Familial differences in the proportion of abnormal hemoglobin present in the sickle cell trait.

The Journal of clinical investigation ·Vol. 30 ·No. 10 ·1951-10-00 ·Pages 1120-4

NEEL JV, WELLS IC, ITANO HA

Abstract

暂无摘要

Keywords

ANEMIA SICKLE CELL/heredity HEMOGLOBIN/abnormalities

MeSH Terms

Anemia Anemia, Sickle Cell/genetics Erythrocytes, Abnormal Hemoglobins/abnormalities Hemoglobins, Abnormal Heredity Humans Sickle Cell Trait

Chemicals

Hemoglobins Hemoglobins, Abnormal

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

NEEL J V

WELLS I C

ITANO H A

References (6)

6 references, click to expand

The occurrence in a family of Sicilian ancestry of the traits for both sickling and thalassemia.
Blood. 1950 Oct;5(10):887-97 PMID: 14772260
A new inherited abnormality of human hemoglobin.
Proc Natl Acad Sci U S A. 1950 Nov;36(11):613-7 PMID: 14808148
Ratio of sickle-cell anemia hemoglobin to normal hemoglobin in sicklemics.
J Biol Chem. 1951 Jan;188(1):65-74 PMID: 14814114
The inheritance of the sickling phenomenon, with particular reference to sickle cell disease.
Blood. 1951 May;6(5):389-412 PMID: 14830636
Sickle cell anemia a molecular disease.
Science. 1949 Nov 25;110(2865):543-8 PMID: 15395398
The Inheritance of Sickle Cell Anemia.
Science. 1949 Jul 15;110(2846):64-6 PMID: 17774955

Article Info

Journal

The Journal of clinical investigation

Abbr.

J Clin Invest

ISSN

0021-9738

DOI

Published

1951-10-00

Pages

1120-4

Language

English

Region

United States

NLM ID

7802877

PMCID

PMC436354

Subset

External Links

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