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Journal Abstract Search

200 related items for PubMed ID: 8116673

  • 1. Newly recognized autosomal recessive faciothoracoskeletal syndrome.
    Richieri-Costa A, Guion-Almeida ML, Lauris JR, Ferreira DM.
    Am J Med Genet; 1994 Jan 15; 49(2):224-8. PubMed ID: 8116673
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  • 2. Marden-Walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consanguineous parents.
    van den Ende JJ, van Bever Y, Rodini ES, Richieri-Costa A.
    Am J Med Genet; 1992 Feb 15; 42(4):467-9. PubMed ID: 1609830
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  • 3. Autosomal recessive malformation syndrome with minor manifestation in the heterozygotes: a preliminary report of a possible new syndrome.
    Paes-Alves AF, Azevêdo ES, Sousa MG, Almeida-Melo N, Oliveira-Filho OJ.
    Am J Med Genet; 1991 Nov 01; 41(2):141-52. PubMed ID: 1785624
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  • 9. Costello syndrome and facio-cutaneous-skeletal syndrome.
    Philip N, Mancini J.
    Am J Med Genet; 1993 Aug 15; 47(2):174-5. PubMed ID: 8213902
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  • 17. Facio-thoraco-genital syndrome: a newly recognized birth defect syndrome.
    Wilf-Miron R, Goodman RM.
    J Craniofac Genet Dev Biol; 1987 Aug 15; 7(1):19-22. PubMed ID: 3597718
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  • 20. Congenital hypothyroidism in Peters plus syndrome.
    Kosaki R, Kamiishi A, Sugiyama R, Kawai M, Hasegawa T, Kosaki K.
    Ophthalmic Genet; 2006 Jun 15; 27(2):67-9. PubMed ID: 16754209
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