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 *

103 related articles for article (PubMed ID: 3355417)

  • 1. Family with aniridia, microcornea, and spontaneously reabsorbed cataract.
    Yamamoto Y; Hayasaka S; Setogawa T
    Arch Ophthalmol; 1988 Apr; 106(4):502-4. PubMed ID: 3355417
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pulverulent cataract with variably associated microcornea and iris coloboma in a MAF mutation family.
    Jamieson RV; Munier F; Balmer A; Farrar N; Perveen R; Black GC
    Br J Ophthalmol; 2003 Apr; 87(4):411-2. PubMed ID: 12642301
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Variable expressivity of autosomal dominant microcornea with cataract.
    Salmon JF; Wallis CE; Murray AD
    Arch Ophthalmol; 1988 Apr; 106(4):505-10. PubMed ID: 3355418
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Juvenile cataract associated with microcornea and glucosuria: a new syndrome].
    Vandekerckhove K; Lange AP; Herzog D; Schipper I
    Klin Monbl Augenheilkd; 2007 Apr; 224(4):344-6. PubMed ID: 17458810
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Morphological and functional findings in a family with aniridia (author's transl)].
    Weber U; Petersen J
    Klin Monbl Augenheilkd; 1981 Jun; 178(6):439-45. PubMed ID: 6973663
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A syndrome involving congenital cataracts of unusual morphology, microcornea, abnormal irides, nystagmus and congenital glaucoma, inherited as an autosomal dominant trait.
    Cebon L; West RH
    Aust J Ophthalmol; 1982 Nov; 10(4):237-42. PubMed ID: 7159305
    [No Abstract]   [Full Text] [Related]  

  • 7. Autosomal dominant cataract and microcornea associated with myopia in a Sicilian family.
    Mollica F; Li Volti S; Tomarchio S; Gangi A; Risiglione V; Gorgone G
    Clin Genet; 1985 Jul; 28(1):42-6. PubMed ID: 4028500
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Aniridia with congenital ptosis and glaucoma: a family study.
    Cohen SM; Nelson LB
    Ann Ophthalmol; 1988 Feb; 20(2):53-7. PubMed ID: 3358595
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2.
    Abouzeid H; Meire FM; Osman I; ElShakankiri N; Bolay S; Munier FL; Schorderet DF
    Ophthalmology; 2009 Jan; 116(1):154-162.e1. PubMed ID: 19004499
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Observations on 5 cases of mesodermic dysgenesis of the cornea and iris in 3 generations of the same family].
    Boles Carenini B; Orzalesi N
    Boll Ocul; 1966 Sep; 45(9):593-618. PubMed ID: 5994237
    [No Abstract]   [Full Text] [Related]  

  • 11. Inherited partial aniridia, microcornea with high myopia and Bergmeister's papilla: a new phenotypic expression.
    Naithani P; Sinha A; Gupta V
    Indian J Ophthalmol; 2008; 56(2):145-6. PubMed ID: 18292626
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal dominant inheritance of iridogoniodysgenesis and cataract.
    Hodes BL; Noecker RJ; Prendiville KJ
    Ophthalmology; 1993 Feb; 100(2):168-72. PubMed ID: 8292106
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital cataract with microcornea and Peters' anomaly as expressions of one autosomal dominant gene.
    Green JS; Johnson GJ
    Ophthalmic Paediatr Genet; 1986 Dec; 7(3):187-94. PubMed ID: 3550563
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Corectopia with nystagmus, absent foveal reflexes and corneal changes.
    Mondino BJ; Cohn HC
    Acta Ophthalmol (Copenh); 1981 Feb; 59(1):85-93. PubMed ID: 7211287
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal dominant cataracts and microcornea.
    Polomeno RC; Cummings C
    Can J Ophthalmol; 1979 Oct; 14(4):227-9. PubMed ID: 550913
    [No Abstract]   [Full Text] [Related]  

  • 16. Variability of iris defects in autosomal dominant aniridia.
    Pearce WG
    Can J Ophthalmol; 1994 Feb; 29(1):25-9. PubMed ID: 8180874
    [No Abstract]   [Full Text] [Related]  

  • 17. An unusual pedigree with microcornea-cataract syndrome.
    Stefaniak E; Zaremba J; Cieślińska I; Kropińska E
    J Med Genet; 1995 Oct; 32(10):813-5. PubMed ID: 8558562
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autosomal dominant keratitis: a possible aniridia variant.
    Pearce WG; Mielke BW; Hassard DT; Climenhaga HW; Climenhaga DB; Hodges EJ
    Can J Ophthalmol; 1995 Apr; 30(3):131-7. PubMed ID: 7627897
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Correlation of different ocular diseases of dominant inheritance. Examination of a family with microcornea, high myopia, retinitis pigmentosa, cataract and glaucoma (author's transl)].
    Schlieter F; Schroeder U
    Klin Monbl Augenheilkd; 1974 Apr; 164(4):485-9. PubMed ID: 4843833
    [No Abstract]   [Full Text] [Related]  

  • 20. [Aniridia in a family characterized by low penetration].
    Balmer A; Zografos L
    J Genet Hum; 1981 Feb; 28(5):195-200. PubMed ID: 7276918
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.