Literature DB >> 13920872

Combinations of high levels of hemoglobin F with haemoglobins A, S, and C in Ghana.

G R THOMPSON, H LEHMANN.   

Abstract

Keywords:  HEMOGLOBIN/abnormalities

Mesh:

Substances:

Year:  1962        PMID: 13920872      PMCID: PMC1958637          DOI: 10.1136/bmj.1.5291.1521

Source DB:  PubMed          Journal:  Br Med J        ISSN: 0007-1447


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  13 in total

1.  Malaria and the sickling trait.

Authors:  A B RAPER
Journal:  Br Med J       Date:  1955-05-14

2.  Expression of the sickle-cell gene in Africa.

Authors:  G M EDINGTON; H LEHMANN
Journal:  Br Med J       Date:  1955-05-28

3.  Significance of haemoglobins S and C in Ghana.

Authors:  G R THOMPSON
Journal:  Br Med J       Date:  1962-03-10

4.  Hereditary persistence of foetal haemoglobin: a family study suggesting allelism of the F gene to the S and C haemoglobin genes.

Authors:  J E MACIVER; L N WENT
Journal:  Br J Haematol       Date:  1961-07       Impact factor: 6.998

5.  Two families showing interaction of haemoglobin C or thalassaemia with high foetal haemoglobin in adults.

Authors:  A P KRAUS; B KOCH; L BURCKETT
Journal:  Br Med J       Date:  1961-05-20

6.  Haemoglobin H disease with persistent haemoglobin "Bart's" in an Oriental Jewess and her daughter: a dual alpha-chain deficiency of human haemoglobin.

Authors:  B RAMOT; C SHEBA; S FISHER; J A AGER; H LEHMANN
Journal:  Br Med J       Date:  1959-12-05

7.  An unusual type of hemoglobinopathy resembling sickle cell-thalassemia disease in a Jamaican family.

Authors:  L N WENT; J E MACIVER
Journal:  Blood       Date:  1958-06       Impact factor: 22.113

8.  Hereditary persistence of foetal haemoglobin production, and its interaction with the sickle-cell trait.

Authors:  G F JACOB; A B RAPER
Journal:  Br J Haematol       Date:  1958-04       Impact factor: 6.998

9.  Protection afforded by sickle-cell trait against subtertian malareal infection.

Authors:  A C ALLISON
Journal:  Br Med J       Date:  1954-02-06

10.  Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

Authors:  K SINGER; A I CHERNOFF; L SINGER
Journal:  Blood       Date:  1951-05       Impact factor: 22.113

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  2 in total

1.  INTERACTION OF BETA-THALASSAEMIA AND HEREDITARY PERSISTENCE OF FOETAL HAEMOGLOBIN.

Authors:  G W BIRD; M I HASAN; O P MALHOTRA; H LEHMANN
Journal:  J Med Genet       Date:  1964-09       Impact factor: 6.318

2.  Sickle-cell anaemia, sickle-cell thalassaemia, sickle-cell haemoglobin C disease, and asymptomatic haemoglobin C thalassaemia in one Ghanaian family.

Authors:  F I Konotey-Ahulu; B Ringelhann
Journal:  Br Med J       Date:  1969-03-08
  2 in total

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