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Journal Abstract Search

90 related items for PubMed ID: 3365105

  • 1. [Marshall syndrome. 2 new cases].
    Nguyen J, Philip N, Arnaud JP, Sibille G, Tisne C, James F.
    Arch Fr Pediatr; 1988 Jan; 45(1):49-51. PubMed ID: 3365105
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  • 2. Multiple branchiogenic anomalies.
    Har-El G, Hadar T, Krespi YP.
    Ear Nose Throat J; 1991 Nov; 70(11):777-82. PubMed ID: 1782888
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  • 3. Oto-palatal-digital syndrome type II with X-linked cerebellar hypoplasia/hydrocephalus.
    Stratton RF, Bluestone DL.
    Am J Med Genet; 1991 Nov 01; 41(2):169-72. PubMed ID: 1785627
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  • 5. Familial mixed deafness with branchial arch defects (earpits-deafness syndrome).
    Slack RW, Phelps PD.
    Clin Otolaryngol Allied Sci; 1985 Oct 01; 10(5):271-7. PubMed ID: 4075550
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  • 11. Marshall syndrome.
    Stratton RF, Lee B, Ramirez F.
    Am J Med Genet; 1991 Oct 01; 41(1):35-8. PubMed ID: 1951461
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  • 13. Hereditary arthro-ophthalmopathy (the Stickler syndrome). Report of a kindred with protrusio acetabuli.
    Beals RK.
    Clin Orthop Relat Res; 1977 Jun 01; (125):32-5. PubMed ID: 880775
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  • 14. Glomerular lesions in the branchio-oto-renal (BOR) syndrome.
    Dumas R, Uziel A, Baldet P, Segond A.
    Int J Pediatr Nephrol; 1982 Jun 01; 3(2):67-70. PubMed ID: 7107121
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  • 15. [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 01; 43(4):250-5. PubMed ID: 3707710
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  • 17. The Stickler syndrome: case reports and literature review.
    Bowling EL, Brown MD, Trundle TV.
    Optometry; 2000 Mar 01; 71(3):177-82. PubMed ID: 10970261
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  • 18. [Genetically determinded deafness; 5 cases of Pendred's syndrome (author's transl)].
    Hörmann K, Held KR.
    HNO; 1980 Jun 01; 28(6):206-8. PubMed ID: 6253416
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