Associated Papers
The roles and regulation of TBX3 in development and disease.
Khan SF et al.
Gene, 2020
Novel TBX3 mutation data in families with ulnar-mammary syndrome indicate a genotype-phenotype relationship: mutations that do not disrupt the T-domain are associated with less severe limb defects.
Meneghini V et al.
European Journal of Medical Genetics, 0
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