Associated Papers
A Synonymous Exonic Splice Silencer Variant in IRF6 as a Novel and Cryptic Cause of Non-Syndromic Cleft Lip and Palate.
Sylvester B et al.
Genes, 2020
Association Between CRISPLD2 Polymorphisms and the Risk of Nonsyndromic Clefts of the Lip and/or Palate: A Meta-analysis.
Ge X et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2018
Galanin pathogenic mutations in temporal lobe epilepsy.
Guipponi M et al.
Human Molecular Genetics, 2015
Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population.
Ludwig KU et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2014
CRISPLD2 variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with or without cleft palate.
Letra A et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2011
Nonsyndromic cleft lip and palate: CRISPLD genes and the folate gene pathway connection.
Chiquet BT et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2011
[Relationship between genetic polymorphisms of MTHFR C677T and nonsyndromic cleft lip with or without palate].
Guo JZ et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences, 2009
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