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Axenfeld-Rieger syndrome: new perspectivesCHANG, Ta C; SUMMERS, C. Gail; SCHIMMENTI, Lisa A et al.British journal of ophthalmology. 2012, Vol 96, Num 3, pp 318-322, issn 0007-1161, 5 p.Article

Syndrome d'Axenfeld-Rieger = Axenfeld-Rieger syndromeSAUER, A; SPEEG-SCHATZ, C.Journal français d'ophtalmologie. 2012, Vol 35, Num 5, issn 0181-5512, p. 392Article

A family with Axenfeld-Rieger syndrome and Peters anomaly caused by a point mutation (Phe112Ser) in the FOXC1 geneHONKANEN, Robert A; NISHIMURA, Darryl Y; SWIDERSKI, Ruth E et al.American journal of ophthalmology. 2003, Vol 135, Num 3, pp 368-375, issn 0002-9394, 8 p.Article

Axenfeld-Rieger syndrome in the age of molecular geneticsALWARD, Wallace L. M.American journal of ophthalmology. 2000, Vol 130, Num 1, pp 107-115, issn 0002-9394Article

Analysis of Mutations of the PITX2 Transcription Factor Found in Patients with Axenfeld-Rieger SyndromeFOOTZ, Tim; IDREES, Faisal; ACHARYA, Moulinath et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 6, pp 2599-2606, issn 0146-0404, 8 p.Article

Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutationsTÜMER, Zeynep; BACH-HOLM, Daniella.European journal of human genetics. 2009, Vol 17, Num 12, pp 1527-1539, issn 1018-4813, 13 p.Article

Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesisBERRY, Fred B; LINES, Matthew A; OAS, J. Martin et al.Human molecular genetics (Print). 2006, Vol 15, Num 6, pp 905-919, issn 0964-6906, 15 p.Article

Axenfeld's anomaly and related disordersTHURSCHWELL, L. M; MICHELSON, M. A.Journal of the American Optometric Association. 1986, Vol 57, Num 5, pp 360-365, issn 0003-0244Article

Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutationMEYER-MARCOTTY, P; WEISSCHUH, N; DRESSLER, P et al.Journal of oral pathology & medicine. 2008, Vol 37, Num 8, pp 504-510, issn 0904-2512, 7 p.Article

Case of chromosome 6p25 terminal deletion associated with axenfeld-rieger syndrome and persistent hyperplastic primary vitreousSUZUKI, Katsuhiro; NAKAMURA, Makoto; AMANO, Emi et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 5, pp 503-508, issn 1552-4825, 6 p.Article

PITX2 and FOXC1 spectrum of mutations in ocular syndromesREIS, Linda M; TYLER, Rebecca C; SEMINA, Elena V et al.European journal of human genetics. 2012, Vol 20, Num 12, pp 1224-1233, issn 1018-4813, 10 p.Article

Reduced human and murine corneal thickness in an axenfeld-rieger syndrome subtypeASAI-COAKWELL, Mika; BACKBOUSE, Christopher; CASEY, Ronald J et al.Investigative ophthalmology & visual science. 2006, Vol 47, Num 11, pp 4905-4909, issn 0146-0404, 5 p.Article

An unusual class of PITX2 mutations in axenfeld-rieger syndromeSAADI, Irfan; TORO, Rafael; KUBURAS, Adisa et al.Birth defects research. Clinical and molecular teratology. 2006, Vol 76, Num 3, pp 175-181, issn 1542-0752, 7 p.Article

Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinctWALTER, M. A; MIRZAYANS, F; MEARS, A. J et al.Ophthalmology (Rochester, MN). 1996, Vol 103, Num 11, pp 1907-1915, issn 0161-6420Article

Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation : A new example of the Chitty syndromeVAN DAELE, S. G; VAN COSTER, R. N; MEIRE, F et al.American journal of medical genetics. 1996, Vol 65, Num 3, pp 205-208, issn 0148-7299Article

Novel mutation in FOXC1 wing region causing Axenfeld-Rieger anomalyPANICKER, Shirty G; SAMPATH, Srirangan; MANDAL, Anil K et al.Investigative ophthalmology & visual science. 2002, Vol 43, Num 12, pp 3613-3616, issn 0146-0404, 4 p.Article

Cardiac valvular disease and Axenfeld-Rieger syndromeTSAI, J. C; GRAJEWSKI, A. L.American journal of ophthalmology. 1994, Vol 118, Num 2, pp 255-256, issn 0002-9394Article

Progressive iris changes in a case of axenfeld-rieger syndromeHONKANEN, Robert; ALWARD, Wallace L. M; COSSARI, Alfred J et al.Archives of ophthalmology (1960). 2006, Vol 124, Num 12, pp 1793-1793, issn 0003-9950, 1 p.Article

Molecular and developmental mechanisms of anterior segment dysgenesisSOWDEN, J. C.Eye (London. 1987). 2007, Vol 21, Num 10, pp 1310-1318, issn 0950-222X, 9 p.Conference Paper

Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with axenfeld-rieger syndrome with developmental glaucomaCELLA, Wener; CABRAI DE VASCONCELLOS, José Paulo; BARBOSA DE MELO, Monica et al.Investigative ophthalmology & visual science. 2006, Vol 47, Num 5, pp 1803-1809, issn 0146-0404, 7 p.Article

A novel (Pro79Thr) mutation in the FKHL7 gene in a Japanese family with Axenfeld-Rieger syndromeSUZUKI, Takefumi; TAKAHASHI, Kana; KUWAHARA, Soichiro et al.American journal of ophthalmology. 2001, Vol 132, Num 4, pp 572-575, issn 0002-9394Article

Anterior chamber cleavage syndrome or mesodermal dysgenesis of the iris and the corneaSCHAUWVLIEGHE, P; DE LAEY, J. J.Bulletin de la Société belge d'ophtalmologie. 1985, Vol 214, pp 113-122, issn 0081-0746Article

Dental and craniofacial anomalies of Axenfeld-Rieger syndromeCHILDERS, N. K; WRIGHT, J. T.Journal of oral pathology. 1986, Vol 15, Num 10, pp 534-539, issn 0300-9777Article

A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomalyWEISSCHUH, N; WOLF, C; WISSINGER, B et al.Clinical genetics. 2008, Vol 74, Num 5, pp 476-480, issn 0009-9163, 5 p.Article

Intravenous patient-controlled analgesia using remifentanil in a child with Axenfeld-Rieger syndromeCOK, Oya Yalcin; OZKOSE, Zerrin; ATABEKOGLU, Serap et al.Paediatric anaesthesia (Paris). 2005, Vol 15, Num 2, pp 162-166, issn 1155-5645, 5 p.Article

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