These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
162 related articles for article (PubMed ID: 416212)
21. 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features. Vande Perre P; Zazo Seco C; Patat O; Bouneau L; Vigouroux A; Bourgeois D; El Hout S; Chassaing N; Calvas P Eur J Med Genet; 2018 Feb; 61(2):72-78. PubMed ID: 29100920 [TBL] [Abstract][Full Text] [Related]
22. Dental anomalies in Axenfeld-Rieger syndrome. O'Dwyer EM; Jones DC Int J Paediatr Dent; 2005 Nov; 15(6):459-63. PubMed ID: 16238657 [TBL] [Abstract][Full Text] [Related]
23. A Novel Mutation of FOXC1 (R127L) in an Axenfeld-Rieger Syndrome Family with Glaucoma and Multiple Congenital Heart Diseases. Du RF; Huang H; Fan LL; Li XP; Xia K; Xiang R Ophthalmic Genet; 2016; 37(1):111-5. PubMed ID: 24914578 [No Abstract] [Full Text] [Related]
24. Familial ectopia lentis with Axenfeld-Rieger anomaly. Singh DV; Sharma YR; Azad RV; Pal N; Gadagina S J Pediatr Ophthalmol Strabismus; 2007; 44(1):59-61. PubMed ID: 17274342 [TBL] [Abstract][Full Text] [Related]
25. Oral manifestations of the Rieger syndrome: report of case. Drum MA; Kaiser-Kupfer MI; Guckes AD; Roberts MW J Am Dent Assoc; 1985 Mar; 110(3):343-6. PubMed ID: 3858346 [TBL] [Abstract][Full Text] [Related]
26. Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma. Pasutto F; Mauri L; Popp B; Sticht H; Ekici A; Piozzi E; Bonfante A; Penco S; Schlötzer-Schrehardt U; Reis A Gene; 2015 Aug; 568(1):76-80. PubMed ID: 25967385 [TBL] [Abstract][Full Text] [Related]
27. [Morphology, family history, and age at diagnosis of 26 patients with Axenfeld-Rieger syndrome and glaucoma or ocular hypertension]. Dressler P; Gramer E Ophthalmologe; 2006 May; 103(5):393-400. PubMed ID: 16683168 [TBL] [Abstract][Full Text] [Related]
28. Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25. Mirzayans F; Gould DB; Héon E; Billingsley GD; Cheung JC; Mears AJ; Walter MA Eur J Hum Genet; 2000 Jan; 8(1):71-4. PubMed ID: 10713890 [TBL] [Abstract][Full Text] [Related]
29. A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma. Micheal S; Siddiqui SN; Zafar SN; Villanueva-Mendoza C; Cortés-González V; Khan MI; den Hollander AI PLoS One; 2016; 11(7):e0160016. PubMed ID: 27463523 [TBL] [Abstract][Full Text] [Related]
31. The Rieger syndrome. Jorgenson RJ; Levin LS; Cross HE; Yoder F; Kelly TE Am J Med Genet; 1978; 2(3):307-18. PubMed ID: 263445 [TBL] [Abstract][Full Text] [Related]
32. Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis. Berry FB; Lines MA; Oas JM; Footz T; Underhill DA; Gage PJ; Walter MA Hum Mol Genet; 2006 Mar; 15(6):905-19. PubMed ID: 16449236 [TBL] [Abstract][Full Text] [Related]
33. Current molecular understanding of Axenfeld-Rieger syndrome. Hjalt TA; Semina EV Expert Rev Mol Med; 2005 Nov; 7(25):1-17. PubMed ID: 16274491 [TBL] [Abstract][Full Text] [Related]
34. Novel mutation in FOXC1 wing region causing Axenfeld-Rieger anomaly. Panicker SG; Sampath S; Mandal AK; Reddy AB; Ahmed N; Hasnain SE Invest Ophthalmol Vis Sci; 2002 Dec; 43(12):3613-6. PubMed ID: 12454026 [TBL] [Abstract][Full Text] [Related]
35. The 6p25 deletion syndrome: An update on a rare neurocristopathy. de Vos IJ; Stegmann AP; Webers CA; Stumpel CT Ophthalmic Genet; 2017; 38(2):101-107. PubMed ID: 27070436 [TBL] [Abstract][Full Text] [Related]
36. Axenfeld-Rieger syndrome: a case report. Dunbar AC; McIntyre GT; Laverick S; Stevenson B J Orthod; 2015; 42(4):324-30. PubMed ID: 26281856 [TBL] [Abstract][Full Text] [Related]
37. [Goniodysplasia in the Bouvier des Flandres]. Rühli MB; Spiess BM Schweiz Arch Tierheilkd; 1996; 138(6):307-11. PubMed ID: 8765546 [TBL] [Abstract][Full Text] [Related]
38. Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report. de la Houssaye G; Bieche I; Roche O; Vieira V; Laurendeau I; Arbogast L; Zeghidi H; Rapp P; Halimi P; Vidaud M; Dufier JL; Menasche M; Abitbol M BMC Med Genet; 2006 Nov; 7():82. PubMed ID: 17134502 [TBL] [Abstract][Full Text] [Related]
39. Primary empty sella and Rieger's anomaly of the anterior chamber of the eye: a familial syndrome. Kleinmann RE; Kazarian EL; Raptopoulos V; Braverman LE N Engl J Med; 1981 Jan; 304(2):90-3. PubMed ID: 7442731 [No Abstract] [Full Text] [Related]
40. Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld-Rieger syndrome. Micheal S; Siddiqui SN; Zafar SN; Venselaar H; Qamar R; Khan MI; den Hollander AI Neurogenetics; 2016 Jan; 17(1):17-23. PubMed ID: 26489929 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]