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Insights into RHCE Molecular Analysis in Samples with Partial D Variants: the Experience of Western France
BACKGROUND: Although systematic blood group genotyping of patients/donors is virtually possible, serological studies remain the gold standard to identify samples of clinical interest that may be further genotyped. In this context, we sought to identify variant D alleles that are likely to be clinica...
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| Foilsithe in: | Transfus Med Hemother |
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| Main Authors: | , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
S. Karger AG
2015
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4698597/ https://ncbi.nlm.nih.gov/pubmed/26733768 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000382086 |
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