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PUBMED FOR HANDHELDS

Journal Abstract Search


68 related items for PubMed ID: 3502790

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  • 3. The Wagner-Stickler syndrome.
    Liberfarb RM, Hirose T.
    Birth Defects Orig Artic Ser; 1982; 18(6):525-38. PubMed ID: 7171772
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  • 7. [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
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  • 8. Clinical features of type 2 Stickler syndrome.
    Poulson AV, Hooymans JM, Richards AJ, Bearcroft P, Murthy R, Baguley DM, Scott JD, Snead MP.
    J Med Genet; 2004 Aug; 41(8):e107. PubMed ID: 15286167
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  • 9. [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
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  • 10. [Spinocerebellar syndrome of early onset associated with retinal degeneration. Report of a case].
    Onsurbe Ramírez I, Lorenzo Sanz G, Aparicio Meix JM.
    An Esp Pediatr; 1990 Oct; 33(4):387-9. PubMed ID: 2278445
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  • 14. A phenotypic variant of Knobloch syndrome.
    Williams TA, Kirkby GR, Williams D, Ainsworth JR.
    Ophthalmic Genet; 2008 Jun; 29(2):85-6. PubMed ID: 18484314
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  • 15. Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect.
    Winterpacht A, Hilbert M, Schwarze U, Mundlos S, Spranger J, Zabel BU.
    Nat Genet; 1993 Apr; 3(4):323-6. PubMed ID: 7981752
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  • 16. [Cartilage-hair hypoplasia--a Finnish growth disorder].
    Mäkitie O.
    Duodecim; 1993 Apr; 109(19):1638-46. PubMed ID: 7736981
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  • 17. [Polyarthritic manifestations revealing Stickler syndrome].
    Hakim H, Elloumi M, Ben Salem M, Karray S, Baklouti S.
    J Radiol; 2002 Dec; 83(12 Pt 1):1856-8. PubMed ID: 12511844
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  • 20. [The heredity of Favre-Goldmann hyaloido-tapeto-retinal degeneration].
    Stanković I, Kecmanović Z, Drincić V.
    Bull Mem Soc Fr Ophtalmol; 1973 Dec; 86(0):246-50. PubMed ID: 4794768
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