All Stories

  1. Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts
  2. ICD-10 impact on ascertainment and accuracy of oral cleft cases as recorded by the Brazilian national live birth information system
  3. Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes
  4. Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate
  5. Analysis of the genetic ancestry of patients with oral clefts from South American admixed populations
  6. Rare nasal cleft in a patient with holoprosencephaly due to a mutation in theZIC2gene