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Journal Abstract Search

154 related items for PubMed ID: 7246605

  • 1. The "long-thumb" brachydactyly syndrome.
    Hollister DW, Hollister WG.
    Am J Med Genet; 1981; 8(1):5-16. PubMed ID: 7246605
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  • 6. Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly.
    Halal F, Picard JL, Raymond-Tremblay D, de Bosset P.
    Am J Med Genet; 1982 Sep; 13(1):71-9. PubMed ID: 7137223
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  • 7. Family study of inherited syndrome with multiple congenital deformities: symphalangism, carpal and tarsal fusion, brachydactyly, craniosynostosis, strabismus, hip osteochondritis.
    Ventruto V, Di Girlamo R, Festa B, Romano A, Sebastio G, Sebastio L.
    J Med Genet; 1976 Oct; 13(5):394-8. PubMed ID: 1003450
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  • 8. Brachydactyly type A1 with abnormal menisci and scoliosis in three generations.
    Raff ML, Leppig KA, Rutledge JC, Weinberger E, Pagon RA.
    Clin Dysmorphol; 1998 Jan; 7(1):29-34. PubMed ID: 9546827
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  • 9. [A new heart defect-brachydactyly syndrome].
    Göblyös P, Czeizel E.
    Orv Hetil; 1989 Oct 01; 130(40):2151-3. PubMed ID: 2616157
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  • 10. Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome?
    Belengeanu V, Rozsnyai K, Farcaş S, Velea I, Fryns JP.
    Genet Couns; 2005 Oct 01; 16(2):167-71. PubMed ID: 16080297
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  • 11. [Emery-Dreifuss disease or syndrome of amyotrophy with early contractures and secondary disorders of cardiac conduction with variable heredity].
    Serratrice G, Pouget J.
    Rev Neurol (Paris); 1986 Oct 01; 142(10):766-70. PubMed ID: 3823708
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  • 12. Variable expression in a dominantly inherited skeletal dysplasia with similarities to brachydactyly E and spondyloepiphyseal-spondyloperipheral dysplasia.
    Sybert VP, Byers PH, Hall JG.
    Clin Genet; 1979 Feb 01; 15(2):160-6. PubMed ID: 104811
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  • 13. Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome.
    Morava E, Czakó M, Kárteszi J, Cser B, Weissbecker K, Méhes K.
    Clin Dysmorphol; 2003 Jul 01; 12(3):161-5. PubMed ID: 14564152
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  • 14. Familial microtia with meatal atresia and conductive deafness in five generations.
    Gupta A, Patton MA.
    Am J Med Genet; 1995 Nov 06; 59(2):238-41. PubMed ID: 8588593
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