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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

243 related articles for article (PubMed ID: 8942889)

  • 1. Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct.
    Walter MA; Mirzayans F; Mears AJ; Hickey K; Pearce WG
    Ophthalmology; 1996 Nov; 103(11):1907-15. PubMed ID: 8942889
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Axenfeld-Rieger syndrome in the age of molecular genetics.
    Alward WL
    Am J Ophthalmol; 2000 Jul; 130(1):107-15. PubMed ID: 11004268
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25).
    Héon E; Sheth BP; Kalenak JW; Sunden SL; Streb LM; Taylor CM; Alward WL; Sheffield VC; Stone EM
    Hum Mol Genet; 1995 Aug; 4(8):1435-9. PubMed ID: 7581385
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformations.
    Lines MA; Kozlowski K; Kulak SC; Allingham RR; Héon E; Ritch R; Levin AV; Shields MB; Damji KF; Newlin A; Walter MA
    Invest Ophthalmol Vis Sci; 2004 Mar; 45(3):828-33. PubMed ID: 14985297
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene.
    Honkanen RA; Nishimura DY; Swiderski RE; Bennett SR; Hong S; Kwon YH; Stone EM; Sheffield VC; Alward WL
    Am J Ophthalmol; 2003 Mar; 135(3):368-75. PubMed ID: 12614756
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic analysis of PITX2 and FOXC1 in Rieger Syndrome patients from Brazil.
    Borges AS; Susanna R; Carani JC; Betinjane AJ; Alward WL; Stone EM; Sheffield VC; Nishimura DY
    J Glaucoma; 2002 Feb; 11(1):51-6. PubMed ID: 11821690
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Axenfeld-Rieger syndrome combined with a foveal anomaly in a three-generation family: a case report.
    Gołaszewska K; Dub N; Saeed E; Mariak Z; Konopińska J
    BMC Ophthalmol; 2021 Mar; 21(1):154. PubMed ID: 33781219
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome.
    Kulak SC; Kozlowski K; Semina EV; Pearce WG; Walter MA
    Hum Mol Genet; 1998 Jul; 7(7):1113-7. PubMed ID: 9618168
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Screening for mutations of Axenfeld-Rieger syndrome caused by FOXC1 gene in Japanese patients.
    Kawase C; Kawase K; Taniguchi T; Sugiyama K; Yamamoto T; Kitazawa Y; Alward WL; Stone EM; Nishimura DY; Sheffield VC
    J Glaucoma; 2001 Dec; 10(6):477-82. PubMed ID: 11740218
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss: a possible new genetic syndrome.
    Cunningham ET; Eliott D; Miller NR; Maumenee IH; Green WR
    Arch Ophthalmol; 1998 Jan; 116(1):78-82. PubMed ID: 9445211
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rieger syndrome.
    Deng J; Wang N
    Yan Ke Xue Bao; 1998 Mar; 14(1):52-6. PubMed ID: 12580078
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. 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]  

  • 19. A new autosomal dominant Peters' anomaly phenotype expanding the anterior segment dysgenesis spectrum.
    Berker N; Alanay Y; Elgin U; Volkan-Salanci B; Simsek T; Akarsu N; Alikasifoglu M
    Acta Ophthalmol; 2009 Feb; 87(1):52-7. PubMed ID: 18616618
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.