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PITX2A
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Body Atlas
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Oral mucosa
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Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Ri…
Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome.
Association Between rs2200733 Polymorphism of PITX2 Gene and the Risk of Atrial Fibrillation.
Corneal Plana-Like Phenotype With Peripheral Scleralization Associated With a Pathogenic Variant of …
Decoding the PITX2-controlled genetic network in atrial fibrillation.
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