Related Experiment Video
Updated: Nov 13, 2025

09:34
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
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The intronic variant RHD:c.149-29G>C designated as RHD*01EL.32 does not cause a DEL phenotype
Tae Yeul Kim1, HongBi Yu2, Duck Cho1,2
1Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Transfusion
|March 15, 2021
Abstract
No abstract available in PubMed .
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