17q12 Knowledge Basedeletion syndrome · static snapshot
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New publication How it is diagnosed 1 supporting source confidence 97% novelty 75%

Clinical and Genetic Significance of Chromosomal Microarray Screening of Asymptomatic Newborns

Introduction In South Korea, low‐resolution chromosomal microarray analysis (LR‐CMA) is frequently used as a screening tool to identify chromosomal anomalies in asymptomatic newborns.

How this was derived

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

Generated 2026-11-14, last changed today. Dedup key newdoc:208. 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)

M., "Novel Microdeletion Syndromes Detected by Chromosome Microarrays," Human Genetics 124, no.

Supporting documents (1)

DocumentSourcePublishedSeenRelevance
Clinical and Genetic Significance of Chromosomal Microarray Screeni... pmc 2026-01-01 yesterday 1.00