DNA from individuals heterozygous for (G)gamma(deltabeta)(o) thalassaemia has been studied by restriction endonuclease analysis. The results reveal a new molecular defect associated with this condition. A total of three defects is now responsible for the one single phenotype, thereby emphasising the complex relationship between genotype and phenotype among the disorders of beta-like globin synthesis in man.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC327644 | PMC |
| http://dx.doi.org/10.1093/nar/9.24.6813 | DOI Listing |
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