The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5'HS4. [electronic resource]
Producer: 20120913Description: 1-5 p. digitalISSN:- 1096-0961
- Adolescent
- Adult
- Alleles
- Case-Control Studies
- Child
- Chromatin -- genetics
- Female
- Genes, Dominant
- Genetic Association Studies
- Genotype
- Heterozygote
- Homozygote
- Humans
- Inverted Repeat Sequences
- Iran
- Linkage Disequilibrium
- Locus Control Region -- genetics
- Male
- Middle Aged
- Mutation
- Phenotype
- Polymorphism, Genetic
- beta-Globins -- chemistry
- beta-Thalassemia -- genetics
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Publication Type: Journal Article
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