Genetic and electrophoretic studies in three Greek families inheriting the traits for both sickling and thalassemia

Author:

Angelopoulos B.

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine,Hematology

Reference20 articles.

1. Zuelzer W. W., J. V. Neel and A. R. Robinson: Abnormal hemoglobins. In Tocantins L. Progress in Hematology New York, Grune and Stratton Inc.,1 (1956).

2. Zuelzer W. W.: Clinical and Haematological aspects of the various haemoglobin syndromes. In Abnormal Hemoglobins, a symposium. Blackwell scientific publications, Oxford 1959.

3. Singer K., L. Singer and S. R. Goldberg: Studies on abnormal hemoglobins XI. Sickle Cell-Thalassemia disease in the negro. The significance of the S+A+F and the S+A patterns obtained by hemoglobin analysis. Blood10, 405 (1955).

4. Silvestroni E. and I. Bianco: Genetic aspects of sickle cell anemia and microdrepanocytic disease. Blood7, 429 (1952).

5. Angelopoulos B.: Unpublished observations.

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