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- W2057647579 abstract "Hemoglobin H (HbH) disease was recently described in three unrelated northern European boys with mental retardation. We have studied a somewhat similar patient, in whom HbH disease was associated with multiple congenital anomalies. Restriction endonuclease analysis of DNA from this proband yielded a pattern consistent with the α-/– genotype commonly associated with the HbH phenotype in Asians. His parents both carry α thalassemia, in contrast to the previously described families in which only one of the two parents was a carrier." @default.
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- W2057647579 date "1982-12-01" @default.
- W2057647579 modified "2023-09-25" @default.
- W2057647579 title "Hemoglobin H disease and multiple congenital anomalies in a child of Northern European origin" @default.
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- W2057647579 doi "https://doi.org/10.1002/ajh.2830130407" @default.
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