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...
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...
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...
The H-2K b gene is a member of the large major histocompatibility complex class I gene family. Since many members of this family cross-hybridize with class I cDNA probes, the cl...
Many eukaryotic genes contain intervening sequences, segments of DNA that interrupt the continuity of the gene. They are removed from RNA transcripts of the gene by a process kn...
h-index: Number of publications with at least h citations each.