A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms. [electronic resource]

By: Contributor(s): Producer: 20180904Description: 685-691 p. digitalISSN:
  • 1537-2995
Subject(s): Online resources: In: Transfusion vol. 58
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Publication Type: Journal Article

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