Associated Papers
Pathogenic Variants in Mennonites From Southern Brazil: Implications for Preventive Measures in Public Health.
Mayer de Lima LB et al.
Clinical Genetics, 2026
Null mutations in Drosophila Optomotor-blind affect T-domain residues conserved in all Tbx proteins.
Sen A et al.
Molecular Genetics and Genomics : Mgg, 2010
TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repression.
Andreou AM et al.
American Journal of Human Genetics, 2007
Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts.
Stanier P et al.
Human Molecular Genetics, 2004
TBX22 mutations are a frequent cause of cleft palate.
Marçano AC et al.
Journal of Medical Genetics, 2004
High incidence of the R276X SALL1 mutation in sporadic but not familial Townes-Brocks syndrome and report of the first familial case.
Kohlhase J et al.
Journal of Medical Genetics, 2003
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.
Braybrook C et al.
Nature Genetics, 2001
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