Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.

We have compared the phenotypes of the two common deletion forms of alpha+-thalassemia by analysis of umbilical cord blood samples from Melanesia. Homozygotes for the leftward, 4.2-kilobase, deletion (-alpha 4.2) had significantly higher levels of Hb Bart's at birth than homozygotes for the rig...

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Hlavní autoři: Bowden, D K, Hill, A V, Higgs, D R, Oppenheimer, S J, Weatherall, D J, Clegg, J B
Médium: Artigo
Jazyk:Inglês
Vydáno: 1987
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC423981/
https://ncbi.nlm.nih.gov/pubmed/3793931
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