QuickView for PITX2;jsessionid=68E538A279AABEFC0B286DC8FE9631AB (gene)

1. Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by…
2. Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Ri…
3. Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome.
4. Association Between rs2200733 Polymorphism of PITX2 Gene and the Risk of Atrial Fibrillation.
5. Corneal Plana-Like Phenotype With Peripheral Scleralization Associated With a Pathogenic Variant of …

There were no clinical trials for PITX2;jsessionid=68E538A279AABEFC0B286DC8FE9631AB