Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng1196-264.pdf
Reference36 articles.
1. Kan, Y.W., Golbus, M.S., Klein, P. & Dozy, A.M. Successful application of prenatal diagnosis in a pregnancy at risk for homozygous β-thalassemia. New Engl. J. Med. 292, 1096–1099 (1975).
2. Kan, Y.W. & Golbus, M.S. and Trecartin, R. Prenatal diagnosis of sickle cell anemia. New Engl. J. Med. 294, 1039–1040 (1976).
3. Ottolenghi, S. et al. The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion. Nature 251, 389–391 (1974).
4. Taylor, J.M. et al. Genetic lesion in homozygous α-thalassaemia (hydrops fetalis). Nature 251, 392–393 (1974).
5. Kan, Y.W., Golbus, M.S. & Dozy, A.M. Prenatal diagnosis of α-thalassemia: Clinical application of molecular hybridization. New Engl. J. Med. 295, 1165–1167 (1976).
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