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.
84 related articles for article (PubMed ID: 3411007)
21. Congenital hypodontia of maxillary lateral incisors in association with coloboma of the iris and hypomaturation type of amelogenesis imperfecta in a large kindred. Atasu M; Eryilmaz A; Genc A; Ozcan M; Ozbayrak S J Clin Pediatr Dent; 1997; 21(4):341-55. PubMed ID: 9484124 [TBL] [Abstract][Full Text] [Related]
22. A newly established mutant strain with mild-type ocular coloboma (retinochoroidal coloboma without microphthalmia) in albino mice. Matsuura T; Kodama Y; Ozaki K; Shirai S; Hirasawa T; Aoyama H; Narama I Birth Defects Res A Clin Mol Teratol; 2006 Apr; 76(4):266-71. PubMed ID: 16596662 [TBL] [Abstract][Full Text] [Related]
23. Exclusion of LCA5 locus in a consanguineous Turkish family with macular coloboma-type LCA. Ozgül RK; Bozkurt B; Kiratli H; Oğüş A Eye (Lond); 2006 Jul; 20(7):817-9. PubMed ID: 16082399 [TBL] [Abstract][Full Text] [Related]
24. Systemic abnormalities associated with iris/nerve head/choroidal/retinal coloboma. Williams TD Optom Vis Sci; 1996 Jul; 73(7):506-10. PubMed ID: 8843132 [TBL] [Abstract][Full Text] [Related]
25. [An analysis of the expression of the mutant angora-Y gene in the mouse]. Koniukhov BV; Berdaliev AS Ontogenez; 1990; 21(5):502-7. PubMed ID: 2280969 [TBL] [Abstract][Full Text] [Related]
26. A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease? Puk O; Esposito I; Söker T; Löster J; Budde B; Nürnberg P; Michel-Soewarto D; Fuchs H; Wolf E; Hrabé de Angelis M; Graw J Invest Ophthalmol Vis Sci; 2009 Sep; 50(9):4311-8. PubMed ID: 19407009 [TBL] [Abstract][Full Text] [Related]
27. Gender-specific alterations in gene expression and loss of liver sexual dimorphism in the long-lived Ames dwarf mice. Amador-Noguez D; Zimmerman J; Venable S; Darlington G Biochem Biophys Res Commun; 2005 Jul; 332(4):1086-100. PubMed ID: 15925325 [TBL] [Abstract][Full Text] [Related]
28. [Expression of the mutant gene mi in mice: white spotting pattern]. Koniukhov BV; Laminina NA Genetika; 1996 Nov; 32(11):1521-7. PubMed ID: 9119213 [TBL] [Abstract][Full Text] [Related]
29. A mouse model for Stickler's syndrome: ocular phenotype of mice carrying a targeted heterozygous inactivation of type II (pro)collagen gene (Col2a1). Kaarniranta K; Ihanamäki T; Sahlman J; Pulkkinen H; Uusitalo H; Arita M; Tammi R; Lammi MJ; Helminen HJ Exp Eye Res; 2006 Aug; 83(2):297-303. PubMed ID: 16546167 [TBL] [Abstract][Full Text] [Related]
30. Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux. Sanyanusin P; Schimmenti LA; McNoe LA; Ward TA; Pierpont ME; Sullivan MJ; Dobyns WB; Eccles MR Nat Genet; 1995 Apr; 9(4):358-64. PubMed ID: 7795640 [TBL] [Abstract][Full Text] [Related]
31. Deletion map of the coloboma (Cm) locus on mouse chromosome 2. Hess EJ; Collins KA; Copeland NG; Jenkins NA; Wilson MC Genomics; 1994 May; 21(1):257-61. PubMed ID: 7916325 [TBL] [Abstract][Full Text] [Related]
32. [Analysis of chimeric mice bearing the fused mutation]. Redina OE; Zhelezova AI; Golubitsa AN; Agul'nik AI; Ruvinskiĭ AO Genetika; 1993 Aug; 29(8):1320-7. PubMed ID: 8405974 [TBL] [Abstract][Full Text] [Related]
33. A population-based case-control study of isolated ocular coloboma. Vogt G; Puhó E; Czeizel AE Ophthalmic Epidemiol; 2005 Jun; 12(3):191-7. PubMed ID: 16036478 [TBL] [Abstract][Full Text] [Related]
34. Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouse. Graw J; Jung M; Löster J; Klopp N; Soewarto D; Fella C; Fuchs H; Reis A; Wolf E; Balling R; Hrabé de Angelis M Genomics; 1999 Nov; 62(1):67-73. PubMed ID: 10585769 [TBL] [Abstract][Full Text] [Related]
36. Phenotypic variability of Cat-Eye syndrome. Berends MJ; Tan-Sindhunata G; Leegte B; van Essen AJ Genet Couns; 2001; 12(1):23-34. PubMed ID: 11332976 [TBL] [Abstract][Full Text] [Related]
37. [Site of fidget gene action and its interaction with the ocular retardation gene in cultured mouse embryo retinas]. Koniukhov BV; Ugol'kova TS Ontogenez; 1978; 9(5):475-80. PubMed ID: 568758 [TBL] [Abstract][Full Text] [Related]
38. A novel candidate gene for mouse and human preaxial polydactyly with altered expression in limbs of Hemimelic extra-toes mutant mice. Clark RM; Marker PC; Kingsley DM Genomics; 2000 Jul; 67(1):19-27. PubMed ID: 10945466 [TBL] [Abstract][Full Text] [Related]
40. Two kinds of ENU-induced scant hair mice and mapping of the mutant genes. Wu BJ; Shao YX; Mao HH; Tang D; Liu J; Xue ZF; Li HD J Dermatol Sci; 2004 Dec; 36(3):149-56. PubMed ID: 15541636 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]