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Journal Abstract Search

126 related items for PubMed ID: 1261064

  • 21. [Multiple lentigines syndrome or leopard syndrome. Presentation of a clinical case].
    Pennelli GM, Guolo S, Pavoncello S, Ferraris AM.
    Minerva Med; 1988 Jul; 79(7):575-8. PubMed ID: 3405460
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  • 22. Multiple lentigines syndrome (LEOPARD syndrome or progressive cardiomyopathic lentiginosis).
    Coppin BD, Temple IK.
    J Med Genet; 1997 Jul; 34(7):582-6. PubMed ID: 9222968
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  • 25. The Noonan syndrome--a review of the clinical and genetic features of 27 cases.
    Collins E, Turner G.
    J Pediatr; 1973 Dec; 83(6):941-50. PubMed ID: 4148394
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  • 28. A study of a family with leopard syndrome.
    Loyd DW, Tsuang MT, Benge JW.
    J Clin Psychiatry; 1982 Mar; 43(3):113-6. PubMed ID: 7061405
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  • 30. Congenital heart disease, deaf-mutism and associated somatic malformations occurring in several members of one family.
    Koroxenidis GT, Webb NC, Moschos CB, Lehan PH.
    Am J Med; 1966 Jan; 40(1):149-55. PubMed ID: 5948041
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  • 32. Leopard syndrome--report of a variant case.
    Munshi A, Munshi AK.
    J Indian Soc Pedod Prev Dent; 1999 Mar; 17(1):5-8. PubMed ID: 10863481
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  • 33. Multiple lentigines syndrome. A case report of a rare familial syndrome with orthopaedic considerations.
    MacEwen GD, Zaharko W.
    Clin Orthop Relat Res; 1973 Mar; (97):34-7. PubMed ID: 4774496
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  • 36. Congenital heart disease and ocular hypertelorism--a new case and a summary of the literature.
    Wang C, Song XL, Yang XD, Zhang C.
    Thorac Cardiovasc Surg; 1984 Jun; 32(3):184-6. PubMed ID: 6206601
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  • 38. Familial Williams syndrome.
    Cortada X, Taysi K, Hartmann AF.
    Clin Genet; 1980 Sep; 18(3):173-6. PubMed ID: 7192194
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  • 40. The spectrum of frontonasal dysplasia in an inbred pedigree.
    Moreno Fuenmayor H.
    Clin Genet; 1980 Feb; 17(2):137-42. PubMed ID: 7363499
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