Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters AnomalyJIANGYUE ZHAO; KAWAI, Kirio; HONGYAN WANG et al.The American journal of pathology. 2012, Vol 180, Num 6, pp 2230-2239, issn 0002-9440, 10 p.Article

Syndrome de Peters : examen biomicroscopique et imagerie du segment antérieur = Peters' syndrome : biomicroscopic, echographic and Scheimpflug examinationATTAL, P; VERA, L; SIAHMED, K et al.Journal français d'ophtalmologie. 2009, Vol 32, Num 4, pp 306-307, issn 0181-5512, 2 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

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

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 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

Peters Plus SyndromeKAPOOR, Seema; SHARMILA BANERJEE MUKHERJEE; ARORA, Ritu et al.Indian journal of pediatrics. 2008, Vol 75, Num 6, pp 635-637, issn 0019-5456, 3 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

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

Anterior Segment Anomalies of the Eye, Growth Retardation Associated With Hypoplastic Pituitary Gland and Endocrine Abnormalities : Jung Syndrome or a New Syndrome?AL-GAZALI, Lihadh; SHATHER, Bedir; KAPLAN, Waleed et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 2, pp 251-256, issn 1552-4825, 6 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

NEWBORN WITH BILATERAL HAZY CORNEASBLEYEN, I; BARTELS, M. C; WOLFS, R. C. W et al.Bulletin de la Société belge d'ophtalmologie. 2007, Num 303, pp 29-32, issn 0081-0746, 4 p.Article

Long-term clinical course and visual outcome associated with Peters' anomalyCHANG, J. W; KIM, J. H; KIM, S.-J et al.Eye (London. 1987). 2012, Vol 26, Num 9, pp 1237-1242, issn 0950-222X, 6 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

LA KÉRATOPLASTIE DANS L'ANOMALIE DE PETERS (CAS CLINIQUE)KAMOUN, B; TURKI, K; KHARRAT, W et al.Bulletin de la Société belge d'ophtalmologie. 2007, Num 303, pp 51-54, issn 0081-0746, 4 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

Peters'-plus syndrome is a congenital disorder of glycosylation caused by a defect in the β1,3-glucosyltransferase that modifies thrombospondin type 1 repeatsHEINONEN, Taisto Y. K; MÄKI, Markku.Annals of medicine (Helsinki). 2009, Vol 41, Num 1, pp 2-10, issn 0785-3890, 9 p.Article