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July 10, 2025Гематология и трансфузиологияOpen Access

A case of rare Del phenotype in a blood donor

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Authors

VKV. V. KaraVDV. V. DaniletsЕRЕ. V. Raykina

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Kara et al. (2025) studied this question.

synapsesocial.com/papers/6a9122d12239ecaee3361789https://doi.org/10.35754/0234-5730-2025-70-2-264-272
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1RHD gene deletion occurred in the Rhesus box2000 · 318 citations
  2. 2Molecular Characteristics of the Serological Weak D Phenotype in Koreans2021 · 8 citations
  3. 3RHCE‐D‐CEhybrid genes can cause false‐negative DNA typing of the Rh e antigen2002 · 6 citations
  4. 4Identification of RHD alleles with the potential of anti‐D immunization among seemingly D− blood donors in Upper Austria2009 · 61 citations
  5. 5Molecular basis of DEL phenotype in the Chinese population2014 · 24 citations