Single-exon fetal RHD genotyping: a 31-month follow up in the obstetric population of Western Sweden.
The single-exon approach for fetal RHD screening early in pregnancy is an appropriate choice in the population of Western Sweden, with a very low frequency of inconclusive results caused by the presence of maternal RHD gene variants. Due to the high sensitivity, specificity, and accuracy of the test, serological typing of neonates born to RhD negative women has no longer been performed at our laboratory since June 2023.
Authors
- Åsa Hellberg (ORCID: https://orcid.org/0000-0002-7000-1899)
- Pauline Isakson (ORCID: https://orcid.org/0000-0001-6363-8288)
- Cecilia Pardi (ORCID: https://orcid.org/0000-0002-0646-7010)
Institutions
- Sahlgrenska University Hospital (SE)
Publication Details
- Journal
- PubMed
- Published
- 2024-09-01
- DOI
- https://doi.org/10.2450/bloodtransfus.741
- Citations
- 1
- Primary Topic
- Prenatal Screening and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 1.11
Funders
- Sahlgrenska Universitetssjukhuset