Associated Papers
Genetic landscape of autism spectrum disorder in Vietnamese children.
Tran KT et al.
Scientific Reports, 2020
Targeted sequencing of cancer-related genes in nasopharyngeal carcinoma identifies mutations in the TGF-β pathway.
Chung AK et al.
Cancer Medicine, 2019
Tooth agenesis and orofacial clefting: genetic brothers in arms?
Phan M et al.
Human Genetics, 2016
27699475 (PubMed )
Supplement: 439_2016_1733_MOESM4_ESM.xlsx › Table_Candidate_Gene_Mutations
Non-syndromic cleft palate: analysis of TBX22 exon 5 gene mutation.
Jiang RS et al.
Archives of Medical Science : Ams, 2012
TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly.
Kaewkhampa A et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2012
Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations.
Kantaputra PN et al.
Journal of Dental Research, 2011
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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