Assessment of candidate genes and genetic heterogeneity in human non syndromic orofacial clefts specifically non syndromic cleft lip with or without palate.

Heliyon · 2019 · PMC6921104 · PMID 31886431

Europe PMC DOI

hedged sentence

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closest p

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boldest claim

The sentences

highly significantno p-value reported

A highly significant association of W185X mutation in PVRL1 was identified in sporadic nonsyndromic CL ± P cases showing heterozygosity pattern ( Sozen et al., 2001 ).

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