<i>RHCE</i> genotyping using next generation sequencing: Allele specific reference sequences
Intronic SNVs may represent a novel alternative diagnostic approach to investigate known and novel variants of the RH genes and the prediction of Rh haplotype.
Authors
- Tracey E. Madgett (ORCID: https://orcid.org/0000-0002-3463-1922)
- Amr J Halawani (ORCID: https://orcid.org/0000-0003-1121-6256)
- Kelly A. Sillence
- Neil D. Avent (ORCID: https://orcid.org/0000-0002-0151-7904)
- Wajnat A. Tounsi (ORCID: https://orcid.org/0000-0002-8536-6989)
- Michele Kiernan (ORCID: https://orcid.org/0000-0002-3940-5385)
Institutions
- King Abdulaziz University (SA)
- Umm al-Qura University (SA)
- Bio-Rad (United Kingdom) (GB)
- University of Plymouth (GB)
Publication Details
- Journal
- Transfusion
- Published
- 2024-12-22
- DOI
- https://doi.org/10.1111/trf.18106
- Citations
- 5
- Primary Topic
- Blood groups and transfusion
- Type
- article
- Field-Weighted Citation Impact
- 2.27
Funders
- King Abdulaziz University