ArticleThe Journal of international medical research2026
Prenatal diagnosis and genetic counseling of a
Article in The Journal of international medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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0 citing papers in PubMed.
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
BackgroundCopy number variations represent a key source of genomic variability, encompassing both benign and pathogenic alterations. Accurate interpretation of copy number variations identified through prenatal screening is critical for effective genetic consultation and clinical management. Microdeletions within the 16q24.3 locus remain understudied, thereby complicating genetic counseling for affected cases.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.