Article
Molecular basis of asymptomatic beta-thalassemia major in an African American individual.
American journal of medical genetics - 17 Mar 1997
Ballas S K, Cai S P, Gabuzda T, Chehab F F
Abstract excerpt
The beta-thalassemia syndromes are a heterogeneous group of genetic disorders characterized by reduced or absent expression of the beta-globin gene. To date, over 300 beta-thalassemia alleles have been characterized in or around the beta-globin region. Thalassemia major is severe anemia necessita...
Topics
- Female
- Haplotypes
- Humans
- Middle Aged
- Mutation
- Nucleic Acid Hybridization
- Polymerase Chain Reaction
- Polymorphism, Genetic
- Syndrome
- beta-Thalassemia
