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2. A variant RhAG protein encoded by the RHAG*572A allele causes serological weak D expression while maintaining normal RhCE phenotypes. Issue 1 (4th October 2018)

4. Genotyping analysis of MNS blood group GP(B‐A‐B) hybrid glycophorins in the Chinese Southern Han population using a high‐resolution melting assay. Issue 7 (13th June 2018)

6. H435‐containing immunoglobulin G3 allotypes are transported efficiently across the human placenta: implications for alloantibody‐mediated diseases of the newborn. Issue 3 (7th July 2013)

9. Identification of a novel frequent RHCE*ce308T variant allele in Chinese D– individuals, resulting in a C+c– phenotype. Issue 9 (24th June 2016)