Associated Papers
Familial hypertrophic cardiomyopathy associated with TBX1 variation.
Zhang J et al.
European Journal of Medical Genetics, 2025
Preliminary investigation into the genetic etiology of short stature in children through whole exon sequencing of the core family.
He J et al.
Open Life Sciences, 2024
Screening for Mutations in the TBX1 Gene on Chromosome 22q11.2 in Schizophrenia.
Ping LY et al.
Genes, 2016
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