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 *

116 related articles for article (PubMed ID: 6801987)

  • 1. Variable expressivity of autosomal dominant anterior segment mesenchymal dysgenesis in six generations.
    Hittner HM; Kretzer FL; Antoszyk JH; Ferrell RE; Mehta RS
    Am J Ophthalmol; 1982 Jan; 93(1):57-70. PubMed ID: 6801987
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and ultrastructural features of a novel hereditary anterior segment dysgenesis.
    Akpek EK; Jun AS; Goodman DF; Green WR; Gottsch JD
    Ophthalmology; 2002 Mar; 109(3):513-9. PubMed ID: 11874753
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel histopathologic finding in the Descemet's membrane of a patient with Peters Anomaly: a case-report and literature review.
    Ni W; Wang W; Hong J; Zhang P; Liu C
    BMC Ophthalmol; 2015 Oct; 15():139. PubMed ID: 26496717
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Anterior chamber cleavage syndrome. A stepladder classification.
    Waring GO; Rodrigues MM; Laibson PR
    Surv Ophthalmol; 1975; 20(1):3-27. PubMed ID: 808872
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Congenital corneal leukomas. 2. Histopathologic findings in 19 eyes with central defect in Descemet's membrane.
    Townsend WM; Font RL; Zimmerman LE
    Am J Ophthalmol; 1974 Feb; 77(2):192-206. PubMed ID: 4405885
    [No Abstract]   [Full Text] [Related]  

  • 8. Anterior segment mesenchymal dysgenesis: probable linkage to the MNS blood group on chromosome 4.
    Ferrell RE; Hittner HM; Kretzer FL; Antoszyk JH
    Am J Hum Genet; 1982 Mar; 34(2):245-9. PubMed ID: 6978612
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteria.
    Hittner HM; Riccardi VM; Ferrell RE; Borda RR; Justice J
    Am J Ophthalmol; 1980 Apr; 89(4):531-9. PubMed ID: 7369316
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Variants of anterior segment dysgenesis and cerebral involvement in a large family with a novel COL4A1 mutation.
    Rødahl E; Knappskog PM; Majewski J; Johansson S; Telstad W; Kråkenes J; Boman H
    Am J Ophthalmol; 2013 May; 155(5):946-53. PubMed ID: 23394911
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital central corneal leukoma (Peters' anomaly).
    Stone DL; Kenyon KR; Green WR; Ryan SJ
    Am J Ophthalmol; 1976 Feb; 81(2):173-93. PubMed ID: 1251879
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Familial congenital cornea guttata with anterior polar cataracts.
    Traboulsi EI; Weinberg RJ
    Am J Ophthalmol; 1989 Aug; 108(2):123-5. PubMed ID: 2757092
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical features of anterior segment dysgenesis associated with congenital corneal opacities.
    Shigeyasu C; Yamada M; Mizuno Y; Yokoi T; Nishina S; Azuma N
    Cornea; 2012 Mar; 31(3):293-8. PubMed ID: 22157569
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal dominantly inherited optic nerve coloboma.
    Yamashita T; Kawano K; Ohba N
    Ophthalmic Paediatr Genet; 1988 Mar; 9(1):17-24. PubMed ID: 3405590
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Heterogeneity in dominant anterior segment malformations.
    Holmström GE; Reardon WP; Baraitser M; Elston JS; Taylor DS
    Br J Ophthalmol; 1991 Oct; 75(10):591-7. PubMed ID: 1954207
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea.
    Devi RR; Vijayalakshmi P
    Mol Vis; 2006 Mar; 12():190-5. PubMed ID: 16604058
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Keratoglobus].
    Pouliquen Y; Dhermy P; Espinasse MA; Savoldelli M
    J Fr Ophtalmol; 1985; 8(1):43-54. PubMed ID: 3889124
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Pseudokeratoconus in trisomy 21 and posterior polymorphous corneal dystrophy].
    Lang GK; Holbach L; Schlötzer U
    Klin Monbl Augenheilkd; 1989 Aug; 195(2):95-9. PubMed ID: 2529395
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of PITX3 mutations in individuals with various ocular developmental defects.
    Zazo Seco C; Plaisancié J; Lupasco T; Michot C; Pechmeja J; Delanne J; Cottereau E; Ayuso C; Corton M; Calvas P; Ragge N; Chassaing N
    Ophthalmic Genet; 2018 Jun; 39(3):314-320. PubMed ID: 29405783
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.