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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

177 related items for PubMed ID: 776247

  • 1.
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  • 2. [Hereditary progressive arthroophthalmopathy (Stickler syndrome)].
    Neuhäuser G.
    Hippokrates; 1976 Feb; 47(1):66-7. PubMed ID: 955946
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  • 4. 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
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  • 8. 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 14; 63(3):461-7. PubMed ID: 8737653
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  • 10. 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 Jun 14; 18(6):539-60. PubMed ID: 7171774
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  • 11. Stickler syndrome in a pedigree of Pierre Robin syndrome.
    Schreiner RL, McAlister WH, Marshall RE, Shearer WT.
    Am J Dis Child; 1973 Jul 14; 126(1):86-90. PubMed ID: 4198747
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  • 13. The arthropathy of hereditary arthroophthalmopathy (Stickler syndrome).
    Lewkonia RM.
    J Rheumatol; 1992 Aug 14; 19(8):1271-5. PubMed ID: 1404165
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  • 14. [Stickler syndrome].
    Alvarez de Santos M, Coronado-Monroy A, Medinilla-Vázquez MG, González-Quiroga G, Ramírez-del Río JL, García-Cervantes ML.
    Bol Med Hosp Infant Mex; 1986 Apr 14; 43(4):250-5. PubMed ID: 3707710
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  • 15. [Stickler syndrome with rhegmatogenous retinal detachment].
    Watanabe H, Kohzaki K, Kubo H, Okano K, Watanabe A, Tsuneoka H.
    Nippon Ganka Gakkai Zasshi; 2010 May 14; 114(5):454-8. PubMed ID: 20545219
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  • 16. The Stickler syndrome: case reports and literature review.
    Bowling EL, Brown MD, Trundle TV.
    Optometry; 2000 Mar 14; 71(3):177-82. PubMed ID: 10970261
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  • 17. [Circular ora avulsion in both eyes with total retinal detachment, vitreo-retinal degeneration and subsequent cataract with high-placed myopia in a child].
    Pfeiffer K, Reim M.
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1978 Mar 14; (75):618-24. PubMed ID: 217335
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  • 20. Stickler syndrome. Presenting as a syndrome of cleft palate, myopia and blindness inherited as a dominant trait.
    Hall J.
    Birth Defects Orig Artic Ser; 1974 Mar 14; 10(8):157-71. PubMed ID: 4218495
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