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Journal Abstract Search

254 related items for PubMed ID: 7189276

  • 1. [49,XXXXY syndrome in a 5-year-old boy].
    Wiśniewski L, Krajewska-Walasek M, Lech H, Mospinek M.
    Pediatr Pol; 1980 Jan; 55(1):81-6. PubMed ID: 7189276
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  • 6. [Median cleft face syndrome. Report of a case].
    Tarateta A, Reboa E, Buffoni L.
    Minerva Pediatr; 1978 Jan 15; 30(1):53-60. PubMed ID: 634250
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  • 10. [The Aarskog syndrome. Description of a case and review of the literature].
    Gemme G, Cordone G, Conforti G, Marchesi A, Lattere M, Bonioli E.
    Minerva Pediatr; 1980 Mar 31; 32(6):393-6. PubMed ID: 6248753
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  • 13. Radioulnar synostosis in Williams syndrome: a historical overview.
    Bzdúch V.
    Am J Med Genet; 1994 May 01; 50(4):386. PubMed ID: 8209922
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  • 14. Congenital radioulnar synostosis, azoospermia, and pseudodicentric Y chromosome.
    Syed AA, Quinton R.
    Fertil Steril; 2008 Aug 01; 90(2):425-6. PubMed ID: 18177653
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  • 16. [A case of neonatal 49,XXXXY syndrome].
    Ságodi L, Lukács V, Lechner E.
    Orv Hetil; 1999 Aug 08; 140(32):1787-90. PubMed ID: 10489762
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