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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

231 related items for PubMed ID: 8766137

  • 21.
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  • 22. Clinical and molecular studies of brachydactyly type D.
    Robin NH, Hurvitz J, Warman ML, Morrison S.
    Am J Med Genet; 1999 Aug 06; 85(4):413-8. PubMed ID: 10398270
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  • 23. Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
    Majewski E, Goecke T, Meinecke P.
    Am J Med Genet; 1996 May 03; 63(1):185-9. PubMed ID: 8723107
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  • 27. Split hand/split foot anomaly in a family segregating a balanced translocation with breakpoint on 7q22.1.
    Genuardi M, Pomponi MG, Sammito V, Bellussi A, Zollino M, Neri G.
    Am J Med Genet; 1993 Nov 01; 47(6):823-31. PubMed ID: 8279479
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  • 28. A new arthrogryposis syndrome with facial and limb anomalies.
    Hall JG, Truog WE, Plowman DL.
    Am J Dis Child; 1975 Jan 01; 129(1):120-2. PubMed ID: 1130329
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  • 29. Familial Gordon syndrome associated with a PIEZO2 mutation.
    Alisch F, Weichert A, Kalache K, Paradiso V, Longardt AC, Dame C, Hoffmann K, Horn D.
    Am J Med Genet A; 2017 Jan 01; 173(1):254-259. PubMed ID: 27714920
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  • 31. Autosomal dominant transmission of acrodysostosis.
    Steiner RD, Pagon RA.
    Clin Dysmorphol; 1992 Oct 01; 1(4):201-6. PubMed ID: 1342871
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  • 33. Vertebral anomalies in a new family with ODED syndrome.
    Piersall LD, Dowton SB, McAlister WH, Waggoner DJ.
    Clin Genet; 2000 Jun 01; 57(6):444-8. PubMed ID: 10905665
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  • 34. Intrafamilial clinical variability in type C brachydactyly.
    Debeer P, De Smet L, Fryns JP.
    Genet Couns; 2001 Jun 01; 12(4):353-8. PubMed ID: 11837604
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  • 37. Tibial hemimelia: report on 37 new cases, clinical and genetic considerations.
    Richieri-Costa A, Ferrareto I, Masiero D, da Silva CR.
    Am J Med Genet; 1987 Aug 01; 27(4):867-84. PubMed ID: 3425598
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  • 40. Autosomal dominant transmission of isolated congenital vertical talus.
    Stern HJ, Clark RD, Stroberg AJ, Shohat M.
    Clin Genet; 1989 Dec 01; 36(6):427-30. PubMed ID: 2591068
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