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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

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

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

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

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

Axenfeld—Rieger Anomaly and Axenfeld—Rieger Syndrome: Clinical, Molecular-Cytogenetic, and DNA Array Analyses of Three Patients With Chromosomal Defects at 6p25TONOKI, Hidefumi; HARADA, Naoki; SHIMOKAWA, Osamu et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 12, pp 2925-2932, issn 1552-4825, 8 p.Article

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