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Updated: Jul 25, 2025

Detection of Residual Donor Erythroid Progenitor Cells after Hematopoietic Stem Cell Transplantation for Patients with Hemoglobinopathies
Published on: September 6, 2017
[RHD Gene Analysis of A Blood Donor with Del Phenotype]
Zhi-Jiang Wang1, Mo-Zhen Peng1, Zhi-Hui Zhang1
1Yunnan Kunming Blood Center, Kunming 650106, Yunnan Province, China.
Objective:
To analyze the RHD genotype of a blood donor with Del phenotype in Yunnan.
Methods:
Rh serological phenotype was identified. RHD gene was detected by PCR-SSP typing, and its 10 exons were sequenced. Exon 9 was amplified for sequencing and analysis. RHD zygosity was detected.
Results:
The Rh phenotype of this specimen was CcDelee. Genomic DNA exhibited a 1 003 bp deletion spanning from intron 8, across exon 9 into intron 9. The deletion breakpoints occurred between two 7-bp short tandem repeat sequences. There was no variation in the sequences of the remaining exons. The Rh hybridization box test showed that there was one RHD negative allele.
Conclusion:
This specimen is Del type caused by deletion of RHD exon 9.
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