Abstract
The Chinese Gγ+(Aγδβ)°-thalassemia is caused by a deletion of more than 80 kilobases. It has a β+-thalassemia phenotype and should be differentiated from other mutations causing β-thalassemia. Using polymerase chain reaction with three oligonucleotide primers bridging the breakpoints, the deletion can be de-tected easily. The method is useful in the genetic counseling and prenatal diag-nosis of the at-risk families.
Original language | English (US) |
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Pages (from-to) | 80-81 |
Number of pages | 2 |
Journal | Acta Haematologica |
Volume | 89 |
Issue number | 2 |
DOIs | |
State | Published - 1993 |
Externally published | Yes |
Keywords
- Beta-thalassemia
- Genetic counseling
- Polymerase chain reaction
- Prenatal diagnosis
ASJC Scopus subject areas
- Hematology