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Analysis of DNA from members of a Melanesian family from Papua New Guinea with haemoglobin (Hb) H disease revealed that all four alpha globin genes are intact in affected subjects. Study of restriction enzyme site and length polymorphisms and the use of oligonucleotide probes indicated that the molecular basis of this Papuan form of non-deletion Hb H disease differs from the previously described Middle Eastern and Mediterranean types.


Journal article


J med genet

Publication Date





767 - 771


Female, Genotype, Humans, Male, Papua New Guinea, Polymorphism, Restriction Fragment Length, Thalassemia