BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

255 related articles for article (PubMed ID: 4020040)

  • 1. [Stickler's syndrome or hereditary progressive arthro-ophthalmopathy].
    Vallat M; Fritsch D; Van Coppenolle F; Detre J; Moze M; Rabourdin F
    J Fr Ophtalmol; 1985; 8(4):301-7. PubMed ID: 4020040
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Stickler's syndrome or hereditary progressive arthro-ophthalmopathy].
    De la Chapelle AC; Manouvrier S; Dubos JP; Farriaux JP
    Pediatrie; 1988; 43(4):305-7. PubMed ID: 3419872
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A dominantly inherited syndrome of hyaloideoretinal degeneration, cleft palate and maxillary hypoplasia (Cervenka syndrome).
    Cohen MM; Knobloch WH; Gorlin RJ
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):83-6. PubMed ID: 5173248
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Stickler syndrome: case reports and literature review.
    Bowling EL; Brown MD; Trundle TV
    Optometry; 2000 Mar; 71(3):177-82. PubMed ID: 10970261
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Stickler's syndrome].
    Goś R; Krawczykowa Z; Trzciński J
    Klin Oczna; 1992 Jan; 94(1):32-3. PubMed ID: 1635370
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Stickler's syndrome. A report of a family.
    Hill JC; Nelson MM
    S Afr Med J; 1989 Mar; 75(5):238-41. PubMed ID: 2928863
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ocular and systemic manifestations of Stickler's syndrome: a preliminary report.
    Weingeist TA; Hermsen V; Hanson JW; Bumsted RM; Weinstein SL; Olin WH
    Birth Defects Orig Artic Ser; 1982; 18(6):539-60. PubMed ID: 7171774
    [No Abstract]   [Full Text] [Related]  

  • 8. The Stickler syndrome (hereditary arthroophthalmopathy).
    Herrmann J; France TD; Spranger JW; Opitz JM; Wiffler C
    Birth Defects Orig Artic Ser; 1975; 11(2):76-103. PubMed ID: 776247
    [No Abstract]   [Full Text] [Related]  

  • 9. A-2-->G transition at the 3' acceptor splice site of IVS17 characterizes the COL2A1 gene mutation in the original Stickler syndrome kindred.
    Williams CJ; Ganguly A; Considine E; McCarron S; Prockop DJ; Walsh-Vockley C; Michels VV
    Am J Med Genet; 1996 Jun; 63(3):461-7. PubMed ID: 8737653
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Stickler's syndrome (hereditary progressive arthro-ophthalmopathy).
    Popkin JS; Polomeno RC
    Can Med Assoc J; 1974 Nov; 111(10):1071-6. PubMed ID: 4429933
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Stickler's syndrome (dystrophia vitreoretinalis hereditaria). Results of surgery for retinal detachment].
    Karel I; Dolezalová J; Oudová P
    Cesk Slov Oftalmol; 2001 May; 57(3):147-54. PubMed ID: 11433587
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Osteochondritis dissecans of the knee in an adult with Stickler syndrome.
    Trepman E
    Orthop Rev; 1993 Mar; 22(3):371-6. PubMed ID: 8474775
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A case of heriditary arthro-ophthalmopathy: Stickler's syndrome].
    Brihaye-Van Geertruyden M; Verlaeken L; Herzeel R; Swinnen MC; Malfroot A
    Bull Soc Belge Ophtalmol; 1979; 183():143-7. PubMed ID: 526682
    [No Abstract]   [Full Text] [Related]  

  • 14. Stickler's syndrome: a study of 12 families.
    Spallone A
    Br J Ophthalmol; 1987 Jul; 71(7):504-9. PubMed ID: 3651362
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Hereditary progressive arthro-ophthalmopathy (Stickler syndrome)].
    Bernd L; Niethard FU; Schiltenwolf M
    Z Orthop Ihre Grenzgeb; 1989; 127(3):358-61. PubMed ID: 2750264
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Hereditary progressive arthroophthalmopathy (Stickler syndrome)].
    Neuhäuser G
    Hippokrates; 1976 Feb; 47(1):66-7. PubMed ID: 955946
    [No Abstract]   [Full Text] [Related]  

  • 17. Congenital myopia in Stickler's hereditary arthro-ophthalmopathy.
    Wang FM; Afran SI; Goldberg RB
    Am J Ophthalmol; 1990 Oct; 110(4):435-6. PubMed ID: 2220987
    [No Abstract]   [Full Text] [Related]  

  • 18. Vitreous veils and radial lattice in Marshall syndrome.
    Brubaker JW; Mohney BG; Pulido JS; Babovic-Vuksanovic D
    Ophthalmic Genet; 2008 Dec; 29(4):184-5. PubMed ID: 19005991
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary arthro-ophthalmopathy (the Stickler syndrome). Report of a kindred with protrusio acetabuli.
    Beals RK
    Clin Orthop Relat Res; 1977 Jun; (125):32-5. PubMed ID: 880775
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital scalp defects and vitreoretinal degeneration: redefining the Knobloch syndrome.
    Seaver LH; Joffe L; Spark RP; Smith BL; Hoyme HE
    Am J Med Genet; 1993 Apr; 46(2):203-8. PubMed ID: 8484411
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.