Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld–Rieger syndrome

By Priston M.  

Human Molecular Genetics, Vol. 10, Iss. 16, 2001-08 ,pp. : 1631-1638

Oxford University Press

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Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld–Rieger syndrome and anterior segment dysgenesis

By Berry Fred B.   Lines Matthew A.   Footz Tim   Underhill D. Alan   Gage Philip J.   Walter Michael A.  

Human Molecular Genetics, Vol. 15, Iss. 6, 2006-03 ,pp. : 905-919

Oxford University Press

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A Rare Recurrent 4q25 Proximal Deletion Not Involving the PITX2 Gene: A Genomic Disorder Distinct from Axenfeld-Rieger Syndrome

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Molecular Syndromology, Vol. 7, Iss. 3, 2016-06 ,pp. : 138-143

Karger

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A molecular basis for differential developmental anomalies in Axenfeld–Rieger syndrome

By Semina E.V.   Espinoza H.M.   Cox C.J.   Amendt B.A.  

Human Molecular Genetics, Vol. 11, Iss. 7, 2002-04 ,pp. : 743-753

Oxford University Press

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Molecular genetics of Axenfeld–Rieger malformations

By Lines1 M.A.   Kozlowski1 K.   Walter1 M.A.  

Human Molecular Genetics, Vol. 11, Iss. 10, 2002-05 ,pp. : 1177-1187

Oxford University Press

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