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8. Rieger syndrome is associated with PAX6 deletion. Riise R; Storhaug K; Brøndum-Nielsen K Acta Ophthalmol Scand; 2001 Apr; 79(2):201-3. PubMed ID: 11284764 [TBL] [Abstract][Full Text] [Related]
9. Multiple congenital anomalies including the Rieger eye malformation in a boy with interstitial deletion of (4) (q25-->q27) secondary to a balanced insertion in his normal father: evidence for haplotype insufficiency causing the Rieger malformation. Schinzel A; Brecevic L; Dutly F; Baumer A; Binkert F; Largo RH J Med Genet; 1997 Dec; 34(12):1012-4. PubMed ID: 9429145 [TBL] [Abstract][Full Text] [Related]
10. Rieger syndrome with de novo reciprocal translocation t(1;4) (q23.1;q25). Makita Y; Masuno M; Imaizumi K; Yamashita S; Ohba S; Ito D; Kuroki Y Am J Med Genet; 1995 May; 57(1):19-21. PubMed ID: 7645592 [TBL] [Abstract][Full Text] [Related]
11. Rieger syndrome: a clinical, molecular, and biochemical analysis. Amendt BA; Semina EV; Alward WL Cell Mol Life Sci; 2000 Oct; 57(11):1652-66. PubMed ID: 11092457 [TBL] [Abstract][Full Text] [Related]
12. [Rieger syndrome as an expression of neural crest dysgenesis]. Lang GE; Fleischer-Peters A Fortschr Ophthalmol; 1989; 86(4):366-9. PubMed ID: 2793009 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. [The Rieger syndrome. A clinical study. A study of 4 generations in one family with the Rieger syndrome]. Rusu V Oftalmologia; 1997; 41(3):234-7. PubMed ID: 9409970 [TBL] [Abstract][Full Text] [Related]
15. Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus. Semina EV; Datson NA; Leysens NJ; Zabel BU; Carey JC; Bell GI; Bitoun P; Lindgren C; Stevenson T; Frants RR; van Ommen G; Murray JC Am J Hum Genet; 1996 Dec; 59(6):1288-96. PubMed ID: 8940274 [TBL] [Abstract][Full Text] [Related]
16. Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome? Grosso S; Farnetani MA; Berardi R; Vivarelli R; Vanni M; Morgese G; Balestri P Am J Med Genet; 2002 Aug; 111(2):182-6. PubMed ID: 12210347 [TBL] [Abstract][Full Text] [Related]
17. Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4. Murray JC; Bennett SR; Kwitek AE; Small KW; Schinzel A; Alward WL; Weber JL; Bell GI; Buetow KH Nat Genet; 1992 Sep; 2(1):46-9. PubMed ID: 1303248 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Rieger syndrome locus: a new reciprocal translocation t(4;12)(q25;q15) and a deletion del(4)(q25q27) both break between markers D4S2945 and D4S193. Flomen RH; Gorman PA; Vatcheva R; Groet J; Barisić I; Ligutić I; Sheer D; Nizetić D J Med Genet; 1997 Mar; 34(3):191-5. PubMed ID: 9132488 [TBL] [Abstract][Full Text] [Related]
20. A novel PITX2 mutation and a polymorphism in a 5-generation family with Axenfeld-Rieger anomaly and coexisting Fuchs' endothelial dystrophy. Kniestedt C; Taralczak M; Thiel MA; Stuermer J; Baumer A; Gloor BP Ophthalmology; 2006 Oct; 113(10):1791.e1-8. PubMed ID: 16876867 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]