BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 3494881)

  • 1. [Hereditary diseases with lens dislocation: clinical aspects].
    Koepp P
    Klin Monbl Augenheilkd; 1987 Jan; 190(1):8-10. PubMed ID: 3494881
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetics of ectopia lentis.
    Sadiq MA; Vanderveen D
    Semin Ophthalmol; 2013; 28(5-6):313-20. PubMed ID: 24138040
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The eye in the Marfan syndrome.
    Maumenee IH
    Birth Defects Orig Artic Ser; 1982; 18(6):515-24. PubMed ID: 6983370
    [No Abstract]   [Full Text] [Related]  

  • 4. The connective tissue.
    Arthritis Rheum; 1970; 13(5):603-15. PubMed ID: 4249402
    [No Abstract]   [Full Text] [Related]  

  • 5. Heritable disorders of connective tissue.
    JAMA; 1973 Apr; 224(5 Suppl):774-6. PubMed ID: 4266956
    [No Abstract]   [Full Text] [Related]  

  • 6. [Marfan syndrome].
    Liska V
    Cesk Slov Oftalmol; 1997 Feb; 53(1):40-5. PubMed ID: 9213523
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic heterogeneity in connective-tissue disorders.
    Lancet; 1971 May; 1(7706):960. PubMed ID: 4102286
    [No Abstract]   [Full Text] [Related]  

  • 8. The classification of heritable disorders of connective tissue.
    McKusick VA
    Birth Defects Orig Artic Ser; 1975; 11(6):1-9. PubMed ID: 811273
    [No Abstract]   [Full Text] [Related]  

  • 9. Weill-Marchesani syndrome in mother and son.
    Young ID; Fielder AR; Casey TA
    Clin Genet; 1986 Dec; 30(6):475-80. PubMed ID: 3493095
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial pseudomarfanism, a new syndrome?
    Dinno ND; Shearer L; Weisskopf B
    Birth Defects Orig Artic Ser; 1979; 15(5B):179-88. PubMed ID: 316715
    [No Abstract]   [Full Text] [Related]  

  • 11. Diagnosing Marfan's syndrome.
    Savige J
    Br Med J (Clin Res Ed); 1988 Jun; 296(6638):1740. PubMed ID: 3135906
    [No Abstract]   [Full Text] [Related]  

  • 12. Ectopia lentis.
    Nelson LB; Maumenee IH
    Surv Ophthalmol; 1982; 27(3):143-60. PubMed ID: 6984233
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Weill-Marchesani syndrome].
    Herrera J; Morales M
    Rev Chil Pediatr; 1986; 57(6):571-2. PubMed ID: 3499643
    [No Abstract]   [Full Text] [Related]  

  • 14. Genetic counseling of families with Marfan syndrome and other disorders showing a Marfanoid body habitus.
    Bard LA
    Ophthalmology; 1979 Oct; 86(10):1764-93. PubMed ID: 317927
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bilateral ametropic functional amblyopia in genetic ectopia lentis: its relation to the amount of subluxation, an indicator for early surgical management.
    Romano PE; Kerr NC; Hope GM
    Binocul Vis Strabismus Q; 2002; 17(3):235-41. PubMed ID: 12171598
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Bilateral posterior lens dislocation in Marfan's syndrome.
    Kumar A; Garg SP; Verma L; Kumar S
    Indian J Ophthalmol; 1989; 37(4):202-4. PubMed ID: 2638316
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hereditary ectopia lentis. A series of 10 cases of ectopia lentis et pupillae.
    Meire FM
    Bull Soc Belge Ophtalmol; 1991; 241():25-36. PubMed ID: 1840993
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A forme fruste of Marfan's syndrome presenting with ectopia lentis and late systolic click.
    Mengesha B
    Ethiop Med J; 1983 Jul; 21(3):181-3. PubMed ID: 6603974
    [No Abstract]   [Full Text] [Related]  

  • 19. Connective tissue disease: closing on the threshold.
    Robinson A
    CMAJ; 1993 Oct; 149(7):988-91. PubMed ID: 8402427
    [No Abstract]   [Full Text] [Related]  

  • 20. Familial Ectopia Lentis: Looking Beyond Marfan's Syndrome.
    Hussain SJ; Amalnath D; Kasthuri N; Subramaniyan VK
    J Assoc Physicians India; 2023 Nov; 71(11):94-95. PubMed ID: 38720505
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.