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.


PUBMED FOR HANDHELDS

Journal Abstract Search


92 related items for PubMed ID: 3238297

  • 1. [Stickler syndrome. Apropos of a case].
    Ziegler G, Gastaud P, Euller-Ziegler L, De Galleani B.
    Rev Rhum Mal Osteoartic; 1988 Dec; 55(12):1009-10. PubMed ID: 3238297
    [No Abstract] [Full Text] [Related]

  • 2. [Goldman-Favre hyaloid-tapeto-retinal degeneration].
    Neetens A, Burvenich H, Hendrata Y, Van Rompaey J, Hofkens R.
    Bull Mem Soc Fr Ophtalmol; 1980 Dec; 92():185-90. PubMed ID: 6971684
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Hereditary vitreoretinal degenerations.
    Neetens A.
    Bull Soc Belge Ophtalmol; 1987 Dec; 223 Pt 2():9-16. PubMed ID: 3502798
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Kniest (Wagner-Stickler variant) and Goldmann-Favre disease in one sibship.
    Neetens A.
    Bull Soc Belge Ophtalmol; 1987 Dec; 223 Pt 2():27-32. PubMed ID: 3502790
    [No Abstract] [Full Text] [Related]

  • 7. Leri-Weill syndrome (dyschondrosteosis): a family study.
    Mohan V, Gupta RP, Helmi K, Marklund T.
    J Hand Surg Br; 1988 Feb; 13(1):16-8. PubMed ID: 3361200
    [Abstract] [Full Text] [Related]

  • 8. [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 Feb; 8(4):301-7. PubMed ID: 4020040
    [Abstract] [Full Text] [Related]

  • 9. A family with vitreo-tapeto-retino-choroidal degeneration with dominant transmission.
    Wille H.
    Acta Ophthalmol (Copenh); 1980 Feb; 58(1):148-57. PubMed ID: 6967673
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Epiphyseal dysplasia of the femoral head, mild vertebral abnormality, myopia, and sensorineural deafness: report of a pedigree with autosomal dominant inheritance.
    MacDermot KD, Roth SC, Hall C, Winter RM.
    J Med Genet; 1987 Oct; 24(10):602-8. PubMed ID: 3681905
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. [Autosome dominant vitreoretinal dystrophy with skeletal dysplasia in one generation].
    Lang GE, Laudi B, Pfeiffer RA.
    Klin Monbl Augenheilkd; 1991 Mar; 198(3):207-14. PubMed ID: 2056740
    [Abstract] [Full Text] [Related]

  • 20. Acromesomelic dysplasia associated with mild lumbar spine stenosis.
    Haliloglu M, Ozen H, Kocak N, Unsal M.
    Eur Radiol; 1999 Mar; 9(1):103-4. PubMed ID: 9933391
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 5.