Cornea with Peters' anomaly: Perturbed Differentiation of Corneal cells and abnormal extracellular matrix in the Corneal stromaOHKAWA, Kiyomi; SAIKA, Shizuya; HAYASHI, Yuko et al.Japanese journal of ophthalmology. 2003, Vol 47, Num 4, pp 327-331, issn 0021-5155, 5 p.Article

Molecular characterization of a familial translocation implicates disruption of HDAC9 and possible position effect on TGFβ2 in the pathogenesis of peters' anomalyDAVID, Dezso; CARDOSO, Joana; MARQUES, Barbara et al.Genomics (San Diego, Calif.). 2003, Vol 81, Num 5, pp 489-503, issn 0888-7543, 15 p.Article

Two novel mutations of the PAX6 gene causing different phenotype in a cohort of Chinese patientsZHANG, X; TONG, Y; XU, W et al.Eye (London. 1987). 2011, Vol 25, Num 12, pp 1581-1589, issn 0950-222X, 9 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

Mutation Analysis of B3GALTL in Peters Plus SyndromeREIS, Linda M; TYLER, Rebecca C; BERGNER, Amanda et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 20, pp 2603-2610, issn 1552-4825, 8 p.Article

CLINICAL SPECTRUM OF CONGENITAL CORNEAL STAPHYLOMA: A CASE REPORTVERSCHOOTEN, R; FOETS, B; DE RAVEL, T et al.Bulletin de la Société belge d'ophtalmologie. 2011, Num 318, pp 7-10, issn 0081-0746, 4 p.Article

Cerebrovasculopathy in NF1 Associated With Ocular and Scalp DefectsSMITH, Matt; HERAN, Manraj K. S; CONNOLLY, Mary B et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 2, pp 380-385, issn 1552-4825, 6 p.Article

A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomalyDOUCETTE, Lance; GREEN, Jane; FERNANDEZ, Bridget et al.European journal of human genetics. 2011, Vol 19, Num 3, pp 293-299, issn 1018-4813, 7 p.Article

Brachymesomelic Dysplasia With Peters Anomaly of the Eye Results From Disruptions of the X Chromosome Near the SHOX and SOX3 GenesBLEYL, Steven B; BYRNE, Janice L. B; CAREY, John C et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 23, pp 2785-2795, issn 1552-4825, 11 p.Article

Prenatal sonographic findings in Peters-plus syndromeBOOG, G; LE VAILLANT, C; JOUBERT, M et al.Ultrasound in obstetrics & gynecology. 2005, Vol 25, Num 6, pp 602-606, issn 0960-7692, 5 p.Article

Continuous expression of the homeobox gene Pax6 in the ageing human retinaSTANESCU, D; ISELI, H. P; SCHWERDTFEGER, K et al.Eye (London. 1987). 2007, Vol 21, Num 1, pp 90-93, issn 0950-222X, 4 p.Article

Exclusion of a PAX6, FOXC1, PITX2, and MYCN Mutation in Another Patient With Apple Peel Intestinal Atresia, Ocular Anomalies and Microcephaly and Review of the LiteratureVAN BEVER, Yolande; VAN HEST, Liselotte; WOLFS, Roger et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 4, pp 500-504, issn 1552-4825, 5 p.Article

Pediatric KeratoplastyVANATHI, M; PANDA, Anita; VENGAYIL, Sujith et al.Survey of ophthalmology. 2009, Vol 54, Num 2, pp 245-271, issn 0039-6257, 27 p.Article