Weak D type 1.1 exemplifies another complexity in weak D genotyping.
about
DCS-1, DCS-2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule.It's time to phase in RHD genotyping for patients with a serologic weak D phenotype. College of American Pathologists Transfusion Medicine Resource Committee Work Group.Blood group genotyping in Germany.Molecular testing in transfusion medicine.Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management.Molecular basis of D variants in Chinese persons.Weak D type 1, 2 and 3 subtype alleles are rare in the Western French population.Correlation between serology and genetics of weak D types in Denmark.Effective molecular RHD typing strategy for blood donations.The RHCE allele ceSL: the second example for D antigen expression without D-specific amino acids.
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Weak D type 1.1 exemplifies another complexity in weak D genotyping.
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2005 nî lūn-bûn
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2005年の論文
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Weak D type 1.1 exemplifies another complexity in weak D genotyping.
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Weak D type 1.1 exemplifies another complexity in weak D genotyping.
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type
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Weak D type 1.1 exemplifies another complexity in weak D genotyping.
@en
Weak D type 1.1 exemplifies another complexity in weak D genotyping.
@nl
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Weak D type 1.1 exemplifies another complexity in weak D genotyping.
@en
Weak D type 1.1 exemplifies another complexity in weak D genotyping.
@nl
P2093
P2860
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Weak D type 1.1 exemplifies another complexity in weak D genotyping.
@en
P2093
Andrea Doescher
Eduard K Petershofen
Franz F Wagner
Ursula Bauerfeind
Willy A Flegel
P2860
P304
P356
10.1111/J.1537-2995.2005.00585.X
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2005-10-01T00:00:00Z