Article

<i>“mir152</i> hypomethylation, potentially triggered by embryonic hypoxia, as a common mechanism for non-syndromic cleft lip/palate”

2019-11-22

Abstract excerpt

Non-syndromic cleft lip/palate (NSCLP), the most common human craniofacial malformations, is a complex disorder given its genetic heterogeneity and multifactorial component revealed by genetic, epidemiological and epigenetic findings. Association of epigenetic variations with NSCLP has been made, however still of little functional investigation. Here we combined a reanalysis of NSCLP methylome data with genetic an...

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Literature Corpus work: 745b4973-f0e1-53b0-9ff3-6074c8c1e1c0
DOI: 10.1101/850016

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