Genetic Study of a Family Possessing Hemoglobins S and C, and Classical Thalassemia.

American journal of human genetics ·Vol. 13 ·No. 4 ·1961-12-00 ·Pages 390-5

McCurdy PR, Pearson HA

Abstract

暂无摘要

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

McCurdy P R

Pearson H A

References (10)

10 references, click to expand

Allelomorphism and the chemical differences of the human haemoglobins A, S and C.
Nature. 1958 Apr 12;181(4615):1062-3 PMID: 13541361
Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.
Blood. 1951 May;6(5):413-28 PMID: 14830637
Genetic basis of the thalassaemia diseases.
Nature. 1959 Dec 19;184:1903-9 PMID: 13852871
Starch block electrophoresis of hemoglobin.
U S Armed Forces Med J. 1959 Jun;10(6):693-700 PMID: 13659734
Qualitative and quantitative control of adult hemoglobin synthesis; a multiple allele hypothesis.
Am J Hum Genet. 1953 Mar;5(1):34-45 PMID: 13050608
The diagnosis of thalassemia trait by starch block electrophoresis of the hemoglobin.
Blood. 1958 Jan;13(1):61-9 PMID: 13499581
Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin.
Nature. 1957 Aug 17;180(4581):326-8 PMID: 13464827
Observations on the inheritance of sickle-cell hemoglobin and hemoglobin C.
J Clin Invest. 1954 Dec;33(12):1634-41 PMID: 13211820
Haemoglobin synthesis in thalassaemia; in-vitro studies.
Br J Haematol. 1959 Jan;5(1):102-20 PMID: 13628932
Identity of haemoglobin A2.
Nature. 1960 Dec 10;188:949-50 PMID: 13726692

Article Info

Journal

American journal of human genetics

Abbr.

Am J Hum Genet

ISSN

0002-9297

Published

1961-12-00

Pages

390-5

Language

English

Region

United States

NLM ID

0370475

PMCID

PMC1932131

External Links

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