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The effects of alpha‐thalassaemia in HbSC disease

Data up to Jan 2025

Published1983
Citations26
References31

Total Citations Per Year

Abstract

References (31)

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1982 • 306 citations

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1982 • 242 citations

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1978 • 241 citations

α-Globin gene organisation in blacks precludes the severe form of α-thalassaemia

1979 • 229 citations

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1975 • 87 citations

A New Sickling Disorder Resulting from Interaction of the Genes for Haemoglobin S and α‐Thalassaemia

1969 • 81 citations

Haematological factors associated with proliferative retinopathy in homozygous sickle cell disease.

1981 • 78 citations

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1973 • 70 citations

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1973 • 61 citations

NEGRO α-THALASSÆMIA IS CAUSED BY DELETION OF A SINGLE α-GLOBIN GENE

1979 • 50 citations

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1981 • 49 citations

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1973 • 47 citations

Molecular Genetics of Human Hemoglobin Synthesis

1979 • 46 citations

Benign Obstetric History in Women with Sickle-cell Anaemia Associated with -Thalassaemia

1972 • 44 citations

Clinical, hematologic and biosynthetic studies in sickle cell‐β°‐thalassemia: A comparison with sickle cell anemia

1976 • 30 citations

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1978 • 30 citations

The association of sickle cell anemia with heterozygous and homozygous α‐thalassemia‐2: In vitro HB chain synthesis

1979 • 29 citations

Failure of the alpha-thalassemia gene to decrease the severity of sickle cell anemia

1978 • 21 citations

Ocular Manifestations in Sickle Cell Disease

1974 • 20 citations

Alpha-Thalassemia-2 and the Variability of Hematological Values in Children with Sickle Cell Anemia

1981 • 19 citations

Henoglobin S-O ARAB-α-Thalassenia Globin Biosynmesis and Clinical Picture

1977 • 14 citations

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1976 • 12 citations

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1974 • 4 citations

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The effects of alpha‐thalassaemia in HbSC disease (1983) – British Journal of Haematology | Metascience Observatory Explorer