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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

126 related items for PubMed ID: 1261064

  • 41.
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    [No Abstract] [Full Text] [Related]

  • 42. Male to male transmission of the G syndrome.
    Farndon PA, Donnai D.
    Clin Genet; 1983 Dec; 24(6):446-8. PubMed ID: 6652958
    [Abstract] [Full Text] [Related]

  • 43. Familial pulmonary stenosis with underdeveloped or normal right ventricle.
    Klinge T, Laursen HB.
    Br Heart J; 1975 Jan; 37(1):60-4. PubMed ID: 1111560
    [Abstract] [Full Text] [Related]

  • 44.
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  • 45.
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  • 47. LEOPARD syndrome without hearing loss or pulmonary stenosis: a report of 2 cases.
    Ramos-Geldres TT, Dávila-Seijo P, Duat-Rodríguez A, Noguera-Morel L, Ezquieta-Zubicaray B, Rosón-López E, Hernández-Martín A, Torrelo-Fernández A.
    Actas Dermosifiliogr; 2015 May; 106(4):e19-22. PubMed ID: 25544017
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  • 48.
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  • 49. The hypertelorism-hypospadias syndrome.
    Reed MH, Shokeir MH, Macpherson RI.
    J Can Assoc Radiol; 1975 Dec; 26(4):240-8. PubMed ID: 1223121
    [Abstract] [Full Text] [Related]

  • 50. [The Leopard syndrome. Description of a case].
    Isaia B, Vivalda L, Spada A.
    Minerva Pediatr; 1982 Feb 15; 34(3):117-24. PubMed ID: 6804773
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  • 51.
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  • 53. Congenital deafness and multiple lentigines. A report of cases in a mother and daughter.
    Capute AJ, Rimoin DL, Konigsmark BW, Esterly NB, Richardson F.
    Arch Dermatol; 1969 Aug 15; 100(2):207-13. PubMed ID: 5797963
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  • 54.
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  • 55. [Greig's syndrome or Pehu's essential hypertelorism syndrome].
    Giovannucci Uzielli ML, Bettini F, Carattoli MT, Maffei G.
    Minerva Pediatr; 1979 Jul 15; 31(13):1015-22. PubMed ID: 481368
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  • 56. Partial agenesis of corpus callosum in LEOPARD syndrome.
    Bonioli E, Di Stefano A, Costabel S, Bellini C.
    Int J Dermatol; 1999 Nov 15; 38(11):855-62. PubMed ID: 10583620
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  • 57. Dominant inheritance of the complex of myxomas, spotty pigmentation, and endocrine overactivity.
    Carney JA, Hruska LS, Beauchamp GD, Gordon H.
    Mayo Clin Proc; 1986 Mar 15; 61(3):165-72. PubMed ID: 3945116
    [Abstract] [Full Text] [Related]

  • 58. [A rare case: association of Waardenburg's syndrome with Greig's hypertelorism].
    Silenzi M.
    Riv Clin Pediatr; 1968 Mar 15; 81(4):321-38. PubMed ID: 5759709
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  • 59.
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  • 60.
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