Immunohistochemical studies of Peter's anomalyCHIA-FWU LEE; YUE, B. Y. J. T; ROBIN, J et al.Ophthalmology (Rochester, MN). 1989, Vol 96, Num 7, pp 958-964, issn 0161-6420Article

Syndrome de Peters: étio-pathogénie et traitement. A propos d'un cas = Peters' syndrome: etiopathogeny and treatment. About one caseFAGART, C; LEBRETON, P; DESJARDINS, L et al.Bulletin des sociétés d'ophtalmologie de France. 1988, Vol 88, Num 1, pp 119-122, issn 0081-1270Article

Unilateral peters' syndromeEVENS, P; NEETENS, I; NEETENS, A et al.Bulletin de la Société belge d'ophtalmologie. 1987, Vol 224, pp 27-37, issn 0081-0746Article

Peters' anomaly as a consequence of genetic and nongenetic syndromesKIVLIN, J. D; FINEMAN, R. M; CRANDALL, A. S et al.Archives of ophthalmology (1960). 1986, Vol 104, Num 1, pp 61-64, issn 0003-9950Article

Ocular and systemic features of Peters' anomalyOZEKI, Hironori; SHIRAI, Shoichiro; NOZAKI, Miho et al.Graefe's archive for clinical and experimental ophthalmology. 2000, Vol 238, Num 10, pp 833-839, issn 0721-832XArticle

Case report : two eyes in one patient representing the spectrum of Peter's anomalyMILLER, B. A; POLLARD, Z. F.Journal of pediatric ophthalmology and strabismus. 1995, Vol 32, Num 6, pp 388-389, issn 0191-3913Article

Peter's anomaly and associated congenital malformationsTRABOULSI, E. I; MAUMENEE, I. H.Archives of ophthalmology (1960). 1992, Vol 110, Num 12, pp 1739-1742, issn 0003-9950Article

Peters plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferaseLESNIK OBERSTEIN, Saskia A. J; KRIEK, Marjolein; WHITE, Stefan J et al.American journal of human genetics. 2006, Vol 79, Num 3, pp 562-566, issn 0002-9297, 5 p.Article

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

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

Growth hormone deficiency (GHD): A new association in Peters' Plus Syndrome (PPS)LEE, Kuk-Wha; LEE, Phillip D. K.American journal of medical genetics. 2004, Vol 124A, Num 4, pp 388-391, issn 0148-7299, 4 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

Surgical management of Glaucoma in infants and children with Peters' anomaly: Long-term structural and functional OutcomeYANG, Lucy L. H; LAMBERT, Scott R; LYNN, Michael J et al.Ophthalmology (Rochester, MN). 2004, Vol 111, Num 1, pp 112-117, issn 0161-6420, 6 p.Article

Anomalie de Peters et pentachromosome X : a propos d'un cas = Peter's anomaly and Penta-X syndrome.One case reportLESUEUR, L; ROLLAND, M; ARNE, J. L et al.Ophtalmologie (Paris). 1994, Vol 8, Num 6, pp 507-509, issn 0989-3105Article

Glaucoma and Peter's anomaly : a clinicopathologic case reportHEATHER HEATH, D; SHIELDS, M. B.Graefe's archive for clinical and experimental ophthalmology. 1991, Vol 229, Num 3, pp 277-280, issn 0721-832X, 4 p.Article

Zur Normogenese der Hornhaut und ihrer Beeinflussung durch Cyclophosphamid im TierexperimentTOST, M; TOST, F.Klinische Monatsblätter für Augenheilkunde. 1990, Vol 197, Num 2, pp 123-127, issn 0023-2165, 5 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

Bilateral Peter's anomaly in an infant with 49,XXXXY syndromeMONAGHAN, K. G; DENNEHY, P. J; VANDYKE, D. L et al.Journal of pediatric ophthalmology and strabismus. 1998, Vol 35, Num 2, pp 112-113, issn 0191-3913Article

Unilateral Peters' anomaly complicated by a corneal tattooPOMELLA, K. M; WAGNER, H.Optometry and vision science. 1998, Vol 75, Num 9, pp 635-639, issn 1040-5488Article

Bilateral penetrating keratoplasty and placement of a Molteno implant in a newborn with Peters' anomalyASTLE, W. F; LIN, D. T. C; DOUGLAS, G. R et al.Canadian journal of ophthalmology. 1993, Vol 28, Num 6, pp 276-282, issn 0008-4182Article

Keratolenticular dysgenesis (Peters' anomaly) as a result of acute embryonic insult during gastrulationCOOK, C. S; SULIK, K. K.Journal of pediatric ophthalmology and strabismus. 1988, Vol 25, Num 2, pp 60-66, issn 0191-3913Article

Atypical Peters' anomaly associated with partial trisomy 5pDICHTL, A; JONAS, J. B; NAUMANN, G. O. H et al.American journal of ophthalmology. 1995, Vol 120, Num 4, pp 541-542, issn 0002-9394Article

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

Optical iridectomy for corneal opacities in Peter's anomalyZAIDMAN, G. W; RABINOWITZ, Y; FORSTOT, S. L et al.Journal of cataract and refractive surgery. 1998, Vol 24, Num 5, pp 719-722, issn 0886-3350Article

PAX 6 is normal in most cases of Peters' anomalyCHURCHILL, A. J; BOOTH, A. P; ANWAR, R et al.Eye (London. 1987). 1998, Vol 12, pp 299-303, issn 0950-222X, 2Article