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Combination of spherocytosis and a variant of beta thalassaemia ('isolated raised Hb A2'). 1967

T A Cunningham, and F Vella

UI MeSH Term Description Entries
D008297 Male Males
D004586 Electrophoresis An electrochemical process in which macromolecules or colloidal particles with a net electric charge migrate in a solution under the influence of an electric current. Electrophoreses
D005796 Genes A category of nucleic acid sequences that function as units of heredity and which code for the basic instructions for the development, reproduction, and maintenance of organisms. Cistron,Gene,Genetic Materials,Cistrons,Genetic Material,Material, Genetic,Materials, Genetic
D006455 Hemoglobins, Abnormal Hemoglobins characterized by structural alterations within the molecule. The alteration can be either absence, addition or substitution of one or more amino acids in the globin part of the molecule at selected positions in the polypeptide chains. Abnormal Hemoglobins
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D013103 Spherocytosis, Hereditary A group of familial congenital hemolytic anemias characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions. Hereditary Spherocytoses,Spherocytoses, Hereditary
D013789 Thalassemia A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia. Thalassemias

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A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia.
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Hb A2 and the diagnosis of beta-thalassaemia trait.
September 1969, The West Indian medical journal,
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Clinical and haematological evaluation of beta thalassaemia intermedia with increased Hb F and Hb A2 in heterozygotes: beta thalassaemia intermedia I.
June 1985, Journal of medical genetics,
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The heterogeneity of normal Hb A2-beta thalassaemia in Greece.
May 1979, British journal of haematology,
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Clinical and haematological evaluation of beta thalassaemia intermedia characterised by unusually low Hb F and increased Hb A2: beta thalassaemia intermedia II.
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The combination of hereditary spherocytosis and heterozygous beta-thalassaemia. A family study.
January 1968, Acta haematologica,
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Interaction of Hb A2 Indonesia trait with beta-thalassaemia trait and with Hb E trait.
January 1978, Acta haematologica,
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Globin gene mapping in normal Hb A2 types of beta-thalassaemia.
May 1982, British journal of haematology,
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Molecular characterization of a normal Hb A2 beta-thalassaemia determinant in a Sardinian family.
October 1987, British journal of haematology,
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A new beta chain variant, Hb Tyne [beta 5(A2)Pro-->Ser].
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