17q12 Knowledge Basedeletion syndrome · static snapshot
All content was collected from public internet sources and processed with the help of AI/LLM software. This site is informative only — do not draw conclusions; verify with the original sources. Full disclaimer
New publication Genes & inheritance 1 supporting source confidence 97% novelty 75%

Prenatal genetic detection in foetus with gallbladder size anomalies: cohort study and systematic review of the literature

Objectives The aim of the study was to evaluate the detection rate of genetic abnormalities in cases of foetal gallbladder (FGB) size abnormalities to determine whether these abnormalities justify prenatal diagnosis.

How this was derived

Indexed from **pmc** on 2026-11-13 (relevance 1.00, tier peer_reviewed).

Generated 2026-11-13, last changed yesterday. Dedup key newdoc:387. The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.

Evidence (1 quote)

Identification of four novel large deletions and complex variants in the alpha-globin locus in Chinese population.

Supporting documents (1)

ArticleSourcePublishedSeenRelevance
Prenatal genetic detection in foetus with gallbladder size anomalie... pmc 2024-01-01 yesterday 1.00