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- W2415980360 abstract "This work shows the higher probability for some individuals of having Hp O phenotype: that is, children under twelve, and individual carriers of haemoglobin S (haemoglobin D carriers do not present this characteristic). This observation appears as a confirmation of the hypotheses explaining Hp O phenotype as a consequence of haemolytic anaemia. Besides, the test of two genetic models taking into account both Hp O and Hp21 M phenotypes leads to strong difficulties due to a certain irregularity of haptoglobin genetic system." @default.
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- W2415980360 date "1975-05-21" @default.
- W2415980360 modified "2023-09-23" @default.
- W2415980360 title "[The phenotype Hp O in several African and Central American populations]." @default.
- W2415980360 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/807418" @default.
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