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 *

105 related articles for article (PubMed ID: 7369316)

  • 21. Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12.
    Kerrison JB; Koenekoop RK; Arnould VJ; Zee D; Maumenee IH
    Am J Ophthalmol; 1998 Jan; 125(1):64-70. PubMed ID: 9437315
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Familial cavitary optic disk anomalies: clinical features of a large family with examples of progressive optic nerve head cupping.
    Honkanen RA; Jampol LM; Fingert JH; Moore MD; Taylor CM; Stone EM; Alward WL
    Am J Ophthalmol; 2007 May; 143(5):788-794. PubMed ID: 17362864
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Concentric macular rings sign in patients with foveal hypoplasia.
    Cornish KS; Reddy AR; McBain VA
    JAMA Ophthalmol; 2014 Sep; 132(9):1084-8. PubMed ID: 24945710
    [TBL] [Abstract][Full Text] [Related]  

  • 25. DNA diagnosis in a family with autosomal dominant aniridia.
    Verbraak FD; Mannens MA; Redeker EJ; Saunders GF; Bleeker-Wagemakers EM
    Ophthalmic Paediatr Genet; 1991 Dec; 12(4):165-70. PubMed ID: 1815167
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical study of a large family with autosomal dominant progressive cone degeneration.
    Small KW; Gehrs K
    Am J Ophthalmol; 1996 Jan; 121(1):1-12. PubMed ID: 8554074
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Non-invasive anterior segment and posterior segment optical coherence tomography and phenotypic characterization of aniridia.
    Gregory-Evans K; Cheong-Leen R; George SM; Xie J; Moosajee M; Colapinto P; Gregory-Evans CY
    Can J Ophthalmol; 2011 Aug; 46(4):337-44. PubMed ID: 21816254
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Butterfly-shaped pigment dystrophy of the fovea.
    Deutman AF; van Blommestein JD; Henkes HE; Waardenburg PJ; Solleveld-van Driest E
    Arch Ophthalmol; 1970 May; 83(5):558-69. PubMed ID: 5442145
    [No Abstract]   [Full Text] [Related]  

  • 29. [Hereditary macular degenerations].
    François J
    Ophthalmologica; 1974; 168(6):417-45. PubMed ID: 4603577
    [No Abstract]   [Full Text] [Related]  

  • 30. Familial bilateral optic nerve hypoplasia.
    Hackenbruch Y; Meerhoff E; Besio R; Cardoso H
    Am J Ophthalmol; 1975 Feb; 79(2):314-20. PubMed ID: 1115199
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Congenital aniridia: long-term clinical course, visual outcome, and prognostic factors.
    Chang JW; Kim JH; Kim SJ; Yu YS
    Korean J Ophthalmol; 2014 Dec; 28(6):479-85. PubMed ID: 25435751
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Autosomal dominant foveal hypoplasia and presenile cataracts. A new syndrome.
    O'Donnell FE; Pappas HR
    Arch Ophthalmol; 1982 Feb; 100(2):279-81. PubMed ID: 7065945
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Butterfly-shaped dystrophy of the macula].
    Behrendt S; Wiechens B
    Klin Monbl Augenheilkd; 1996 Jul; 209(1):51-2. PubMed ID: 8965479
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Dominant cystoid macular dystrophy.
    Saksens NT; van Huet RA; van Lith-Verhoeven JJ; den Hollander AI; Hoyng CB; Boon CJ
    Ophthalmology; 2015 Jan; 122(1):180-91. PubMed ID: 25267528
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Glaucoma in aniridia(apparent) or irideremia].
    Sampaolesi R; Reca RM
    Arch Oftalmol B Aires; 1968 Mar; 43(3):31-8. PubMed ID: 5737817
    [No Abstract]   [Full Text] [Related]  

  • 36. Dominant goniodysgenesis with late congenital glaucoma. A re-examination of Berg's pedigree.
    Jerndal T
    Am J Ophthalmol; 1972 Jul; 74(1):28-33. PubMed ID: 4624765
    [No Abstract]   [Full Text] [Related]  

  • 37. Familial hypoplasia of the iris stroma associated with glaucoma.
    Weatherill JR; Hart CT
    Br J Ophthalmol; 1969 Jul; 53(7):433-8. PubMed ID: 5804028
    [No Abstract]   [Full Text] [Related]  

  • 38. Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications.
    Iannaccone A; Kerr NC; Kinnick TR; Calzada JI; Stone EM
    Arch Ophthalmol; 2011 Feb; 129(2):211-7. PubMed ID: 21320969
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fenestrated sheen macular dystrophy.
    Sneed SR; Sieving PA
    Am J Ophthalmol; 1991 Jul; 112(1):1-7. PubMed ID: 1882912
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A new dominant progressive foveal dystrophy.
    Frank HR; Landers MB; Williams RJ; Sidbury JB
    Am J Ophthalmol; 1974 Dec; 78(6):903-16. PubMed ID: 4440724
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.