craniofacial development
National Institutes of Health
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OBJECTIVES
The RASopathies are a group of syndromes that have in common germline mutations in genes that encode components of the…
Defects in mid-facial development, including cleft lip/palate, account for a large number of human birth defects annually. In…
Opitz syndrome (OS) is a genetic disorder that affects mainly the development of midline structures, including the craniofacial…
Objective To determine the association of single-nucleotide polymorphisms (SNPs) in genes related to craniofacial development…
Neural crest cells (NCCs) are a transient, migratory cell population, which originates during neurulation at the neural folds and…
Among human birth defect syndromes, malformations affecting the face are perhaps the most striking due to cultural and…