Associated Papers
Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate.
Leslie EJ et al.
Clinical Genetics, 2013
Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects.
Leoyklang P et al.
Human Mutation, 2007
Medical sequencing of candidate genes for nonsyndromic cleft lip and palate.
Vieira AR et al.
Plos Genetics, 2005
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