Citations (19)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (2)
S.M. Quinn, G.C.M. Black, S. Biswas, J. Clayton-Smith & I.C. Lloyd. (2004) Autosomal dominant brachydactyly, coloboma and anterior segment dysgenesis. Ophthalmic Genetics 25:4, pages 277-283.
Read now
Read now
Simone Finzi, Carla F. Pinto & Janey L. Wiggs. (2001) Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma. Ophthalmic Genetics 22:1, pages 35-41.
Read now
Read now
Articles from other publishers (17)
Jiaxu Hong, Yujing Yang, Claus Cursiefen, Alireza Mashaghi, Dan Wu, Zuguo Liu, Xinghuai Sun, Reza Dana & Jianjiang Xu. (2017) Optimising keratoplasty for Peters' anomaly in infants using spectral-domain optical coherence tomography. British Journal of Ophthalmology 101:6, pages 820-827.
Crossref
Crossref
Yoshio Shima & Makoto Migita. (2016) Prenatal Detection of Peters' Plus Syndrome in a Patient with No Known Family History. Journal of Nippon Medical School 83:3, pages 130-132.
Crossref
Crossref
Darshan Kumar U. Kansara & Sunil G. Biradar. (2015) PETER’S TYPE II ANOMALY ASSOCIATED WITH CONGENITAL HEART DEFECT: RARE CASE REPORT. Journal of Evidence Based Medicine and Healthcare 2:10, pages 1565-1568.
Crossref
Crossref
Chika Shigeyasu, Masakazu Yamada, Yoshinobu Mizuno, Tadashi Yokoi, Sachiko Nishina & Noriyuki Azuma. (2012) Clinical Features of Anterior Segment Dysgenesis Associated With Congenital Corneal Opacities. Cornea 31:3, pages 293-298.
Crossref
Crossref
Helena Lee, Katrina Meyers, Bernadette Lanigan & Michael O’Keefe. (2010) Complications and Visual Prognosis in Children with Aniridia. Journal of Pediatric Ophthalmology & Strabismus 47:4, pages 205-210.
Crossref
Crossref
Lihadh Al-Gazali, Bedir Shather, Waleed Kaplan, Kais Algawi & Bassam R. Ali. (2009) Anterior segment anomalies of the eye, growth retardation associated with hypoplastic pituitary gland and endocrine abnormalities: Jung syndrome or a new syndrome?. American Journal of Medical Genetics Part A 149A:2, pages 251-256.
Crossref
Crossref
Joel Sugar & Hormuz P. Wadia. 2009. Ophthalmology. Ophthalmology
214
218
.
Robert L Stamper, Marc F Lieberman & Michael V Drake. 2009. Becker-Shaffer's Diagnosis and Therapy of the Glaucomas. Becker-Shaffer's Diagnosis and Therapy of the Glaucomas
294
329
.
Antje Wurm, Elisabeth Sock, Rudolf Fuchshofer, Michael Wegner & Ernst R. Tamm. (2008) Anterior segment dysgenesis in the eyes of mice deficient for the high-mobility-group transcription factor Sox11. Experimental Eye Research 86:6, pages 895-907.
Crossref
Crossref
Seema Kapoor, Sharmila Banerjee Mukherjee, Ritu Arora & Daraius Shroff. (2008) Peters plus syndrome. The Indian Journal of Pediatrics 75:6, pages 635-637.
Crossref
Crossref
J. Sánchez Zahonero, M. Andrés Celma & M.ªJ. López García. (2008) Mosaicismo de trisomía 9: caso de larga supervivencia. Anales de Pediatría 68:3, pages 273-276.
Crossref
Crossref
Dany M. Najjar, Stephen P. Christiansen, Erick D. Bothun & C. Gail Summers. (2006) Strabismus and Amblyopia in Bilateral Peters Anomaly. Journal of American Association for Pediatric Ophthalmology and Strabismus 10:3, pages 193-197.
Crossref
Crossref
Mayumi Morimoto, Tomoyuki Takano, Yuko Sakaue, Chihiro Sawai, Hirofumi Aotani, Shigeki Koshida & Yoshihiro Takeuchi. (2004) Peters' anomaly with bilateral perisylvian polymicrogyria and abdominal calcification. Congenital Anomalies 44:2, pages 99-102.
Crossref
Crossref
Kuk‐Wha Lee & Phillip D. K. Lee. (2003) Growth hormone deficiency (GHD): A new association in Peters' plus syndrome (PPS). American Journal of Medical Genetics Part A 124A:4, pages 388-391.
Crossref
Crossref
Liesbeth J.J.M. Maillette de Buy Wenniger-Prick & Raoul C.M. Hennekam. (2002) The Peters’ plus syndrome: a review. Annales de Génétique 45:2, pages 97-103.
Crossref
Crossref
U. Moog, E.M. Bleeker-Wagemakers, P. Crobach, J.S.H. Vles & C.T.R.M. Schrander-Stumpel. (1998) Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: A new autosomal recessive syndrome?. American Journal of Medical Genetics 78:3, pages 263-266.
Crossref
Crossref
Albert Dichtl, Jost B. Jonas & Gottfried O.H. Naumann. (1995) Atypical Peters' Anomaly Associated With Partial Trisomy 5p. American Journal of Ophthalmology 120:4, pages 541-542.
Crossref
Crossref