Prenatal Diagnosis of β-Thalassemia
We investigated a method employing synthetic oligonucleotides for the prenatal diagnosis of beta-thalassemia due to a single nucleotide mutation. The beta 0 thalassemia we teste...
Publications
2 shownα1-Antitrypsin deficiency detection by direct analysis of the mutation in the gene
A deficiency in the plasma protease inhibitor alpha 1-antitrypsin can cause chronic obstructive emphysema or infantile liver cirrhosis. This deficiency results from a single ami...
Frequent Co-Authors
Researcher Info
- h-index
- 2
- Publications
- 2
- Citations
- 470
- Institution
- Baylor College of Medicine
External Links
Impact Metrics
h-index
2
h-index: Number of publications with at least h citations each.