Associated Papers
Broad Next-Generation Integrated Sequencing of Myelofibrosis Identifies Disease-Specific and Age-Related Genomic Alterations.
Kandarpa M et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2024
38386293 (PubMed )
Supplement: ccr-23-0372_supplemental_table_2_suppst2.xlsx › Suppl._Table_2
Non-syndromic cleft palate: analysis of TBX22 exon 5 gene mutation.
Jiang RS et al.
Archives of Medical Science : Ams, 2012
Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations.
Kantaputra PN et al.
Journal of Dental Research, 2011
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 mutations are a frequent cause of non-syndromic cleft palate in the Thai population.
Suphapeetiporn K et al.
Clinical Genetics, 2007
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