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65. PITX2 deficiency and associated human disease: insights from the zebrafish model. Hendee KE; Sorokina EA; Muheisen SS; Reis LM; Tyler RC; Markovic V; Cuturilo G; Link BA; Semina EV Hum Mol Genet; 2018 May; 27(10):1675-1695. PubMed ID: 29506241 [TBL] [Abstract][Full Text] [Related]
66. Pitx2-mediated cardiac outflow tract remodeling. Ma HY; Xu J; Eng D; Gross MK; Kioussi C Dev Dyn; 2013 May; 242(5):456-68. PubMed ID: 23361844 [TBL] [Abstract][Full Text] [Related]
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69. Genetic analysis of PITX2 and FOXC1 in Rieger Syndrome patients from Brazil. Borges AS; Susanna R; Carani JC; Betinjane AJ; Alward WL; Stone EM; Sheffield VC; Nishimura DY J Glaucoma; 2002 Feb; 11(1):51-6. PubMed ID: 11821690 [TBL] [Abstract][Full Text] [Related]
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71. The pitx2 homeobox protein is required early for endoderm formation and nodal signaling. Faucourt M; Houliston E; Besnardeau L; Kimelman D; Lepage T Dev Biol; 2001 Jan; 229(2):287-306. PubMed ID: 11203696 [TBL] [Abstract][Full Text] [Related]
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79. A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes. Idrees F; Bloch-Zupan A; Free SL; Vaideanu D; Thompson PJ; Ashley P; Brice G; Rutland P; Bitner-Glindzicz M; Khaw PT; Fraser S; Sisodiya SM; Sowden JC Am J Med Genet B Neuropsychiatr Genet; 2006 Mar; 141B(2):184-91. PubMed ID: 16389592 [TBL] [Abstract][Full Text] [Related]
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