ArticleFrontiers in genetics2023
Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants.
Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
7 citing papers in PubMed.
- EHA Recommendations for preconceptual and antenatal screening and prenatal diagnosis for hemoglobinopathies.HemaSphere · 2026Article
- Decoding thalassemia and sickle cell disease: advances in molecular technologies for comprehensive variant detection.Frontiers in genetics · 2026Review
- Cord blood-based neonatal genetic screening for thalassemia in Guiyang, China (2015): a cross-sectional study.Frontiers in genetics · 2026Article
- Prevention and control of thalassemia in Guangdong Province, Southern China: insights from an 11-year retrospective study.Annals of medicine · 2025Article
- Detection of a novel large fragment deletion in the alpha-globin gene cluster using the CNVplex technology.Frontiers in genetics · 2025Article
- Current research status of third-generation sequencing technology in thalassemia detection.Frontiers in pediatrics · 2025Review
- Spectrum of Beta-Thalassemia Mutations in Potential Carriers with Microcytic Hypochromic Anemia from Mazandaran and Golestan, Northern Provinces of Iran.BioMed research international · 2024Article
Corrections and comments
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Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
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Registered trials
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