We used in vitro DNA amplification by the polymerase chain reaction and nonradioactive probes for prenatal diagnosis of β thalassemia in Chinese from the Guangdong province. Exact molecular diagnoses were made in all 20 fetuses studied over a 6-month period. We conclude that this method of prenatal diagnosis for β thalassemia is a viable approach in many parts of the world where this disease is common.
CITATION STYLE
Cai, S. P., Chang, C. A., Zhang, J. Z., Saiki, R. K., Erlich, H. A., & Kan, Y. W. (1989). Rapid prenatal diagnosis of β thalassemia using DNA amplification and nonradioactive probes. Blood, 73(2), 372–374. https://doi.org/10.1182/blood.v73.2.372.bloodjournal732372
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