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3. Homonucleotide expansion and contraction mutations of PAX2 and inclusion of Chiari 1 malformation as part of renal-coloboma syndrome. Schimmenti LA; Shim HH; Wirtschafter JD; Panzarino VA; Kashtan CE; Kirkpatrick SJ; Wargowski DS; France TD; Michel E; Dobyns WB Hum Mutat; 1999; 14(5):369-76. PubMed ID: 10533062 [TBL] [Abstract][Full Text] [Related]
4. Autosomal dominant optic nerve colobomas, vesicoureteral reflux, and renal anomalies. Schimmenti LA; Pierpont ME; Carpenter BL; Kashtan CE; Johnson MR; Dobyns WB Am J Med Genet; 1995 Nov; 59(2):204-8. PubMed ID: 8588587 [TBL] [Abstract][Full Text] [Related]
5. Mutation of the gene in a family with optic nerve colobomas, renal anomolies and vesicoureteral reflux. Sanyanusin P; Schimmenti LA; McNoe TA; Ward TA; Pierpont ME; Sullivan MJ; Dobyns WB; Eccles MR Nat Genet; 1996 May; 13(1):129. PubMed ID: 8673093 [No Abstract] [Full Text] [Related]
6. Multicystic dysplastic kidney and variable phenotype in a family with a novel deletion mutation of PAX2. Fletcher J; Hu M; Berman Y; Collins F; Grigg J; McIver M; Jüppner H; Alexander SI J Am Soc Nephrol; 2005 Sep; 16(9):2754-61. PubMed ID: 16049068 [TBL] [Abstract][Full Text] [Related]
7. [Genetic basis for malformation-associated uropathy and renal dysplasia]. Oppezzo C; Barberis V; Edefonti A; Cusi D; Marra G G Ital Nefrol; 2003; 20(2):120-6. PubMed ID: 12746796 [TBL] [Abstract][Full Text] [Related]
8. The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomalies. Cunliffe HE; McNoe LA; Ward TA; Devriendt K; Brunner HG; Eccles MR J Med Genet; 1998 Oct; 35(10):806-12. PubMed ID: 9783702 [TBL] [Abstract][Full Text] [Related]
10. Identification of two single nucleotide polymorphisms in exon 8 of PAX2. Shim HH; Nakamura BN; Cantor RM; Schimmenti LA Mol Genet Metab; 1999 Dec; 68(4):507-10. PubMed ID: 10607481 [TBL] [Abstract][Full Text] [Related]
11. Renal-coloboma syndrome: a single nucleotide deletion in the PAX2 gene at Exon 8 is associated with a highly variable phenotype. Taranta A; Palma A; De Luca V; Romanzo A; Massella L; Emma F; Dello Strologo L Clin Nephrol; 2007 Jan; 67(1):1-4. PubMed ID: 17269592 [TBL] [Abstract][Full Text] [Related]
12. Pax2 in development and renal disease. Dressler GR; Woolf AS Int J Dev Biol; 1999; 43(5):463-8. PubMed ID: 10535325 [TBL] [Abstract][Full Text] [Related]
13. Association of PAX2 and Other Gene Mutations with the Clinical Manifestations of Renal Coloboma Syndrome. Okumura T; Furuichi K; Higashide T; Sakurai M; Hashimoto S; Shinozaki Y; Hara A; Iwata Y; Sakai N; Sugiyama K; Kaneko S; Wada T PLoS One; 2015; 10(11):e0142843. PubMed ID: 26571382 [TBL] [Abstract][Full Text] [Related]
14. Optic nerve dysplasia and renal insufficiency in a family with a novel PAX2 mutation, Arg115X: further ophthalmologic delineation of the renal-coloboma syndrome. Schimmenti LA; Manligas GS; Sieving PA Ophthalmic Genet; 2003 Dec; 24(4):191-202. PubMed ID: 14566649 [TBL] [Abstract][Full Text] [Related]
15. Pax2 expression and retinal morphogenesis in the normal and Krd mouse. Otteson DC; Shelden E; Jones JM; Kameoka J; Hitchcock PF Dev Biol; 1998 Jan; 193(2):209-24. PubMed ID: 9473325 [TBL] [Abstract][Full Text] [Related]
16. The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney. Favor J; Sandulache R; Neuhäuser-Klaus A; Pretsch W; Chatterjee B; Senft E; Wurst W; Blanquet V; Grimes P; Spörle R; Schughart K Proc Natl Acad Sci U S A; 1996 Nov; 93(24):13870-5. PubMed ID: 8943028 [TBL] [Abstract][Full Text] [Related]
17. [Renal-coloboma syndrome]. Asensio Sánchez VM; Corral Azor A; Bartolomé Aragón A; De Paz García M Arch Soc Esp Oftalmol; 2002 Nov; 77(11):635-8. PubMed ID: 12410411 [TBL] [Abstract][Full Text] [Related]
18. Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations. Schimmenti LA; Cunliffe HE; McNoe LA; Ward TA; French MC; Shim HH; Zhang YH; Proesmans W; Leys A; Byerly KA; Braddock SR; Masuno M; Imaizumi K; Devriendt K; Eccles MR Am J Hum Genet; 1997 Apr; 60(4):869-78. PubMed ID: 9106533 [TBL] [Abstract][Full Text] [Related]
19. Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Keller SA; Jones JM; Boyle A; Barrow LL; Killen PD; Green DG; Kapousta NV; Hitchcock PF; Swank RT; Meisler MH Genomics; 1994 Sep; 23(2):309-20. PubMed ID: 7835879 [TBL] [Abstract][Full Text] [Related]