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Author

A. Letra

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Open access Jul 2026

Genome-wide assessment of rare protein-coding variants identifies associations with non-syndromic cleft lip/palate.

Gene-based association testing, meta-analysis, functional prioritization, and effect-size estimation revealed several novel NSCLP candidate genes and confirmed associations with previously reported genes, providing strong support for a polygenic inheritance model in NSCLP.

Yao Yu, G. Kowalczyk, Chad D. Huff et al. · 0 citations

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