There is increasing evidence that genetic risk variants for non-syndromic cleft lip/palate
(nsCL/P) are also associated with normal-range variation in facial morphology. However …

Objectives: Orofacial clefting is one of the most prevalent craniofacial malformations.
Previous research has demonstrated that unaffected relatives of patients with non-syndromic …

Unaffected relatives of individuals with non-syndromic cleft lip with or without cleft palate
(NSCL/P) show distinctive facial features. The presence of this facial endophenotype is …

Nonsyndromic cleft lip with or without cleft palate (nsCL/P) is among the most common
human birth defects with multifactorial etiology. Here, we present results from a genome …

Non-syndromic cleft lip with or without palate (NSCL/P) is a prevalent birth defect that affects
1/500–1/1400 live births globally. The genetic basis of NSCL/P is intricate and involves both …

Non-syndromic cleft lip with or without palate (NSCL/P) is a frequent malformation of the
facial region. Genetic variants (SNPs) within nineteen loci have been previously associated …

We have conducted the first meta-analyses for nonsyndromic cleft lip with or without cleft
palate (NSCL/P) using data from the two largest genome-wide association studies published …

Non-syndromic cleft lip with or without cleft palate (nsCL/P) is a common congenital facial
malformation with a multifactorial etiology. Genome-wide association studies (GWASs) have …

Recent genome-wide association studies have identified single nucleotide polymorphisms
(SNPs) associated with non-syndromic cleft lip with or without cleft palate (NSCL/P), and …

The 3 major subphenotypes observed in patients with nonsyndromic orofacial clefts
(NSOFCs) are nonsyndromic cleft lip only (NSCLO), nonsyndromic cleft lip with palate …