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PUBMED FOR HANDHELDS

Journal Abstract Search


232 related items for PubMed ID: 12657005

  • 1. The ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC): report of five cases.
    Bigatà X, Bielsa I, Artigas M, Azón A, Ribera M, Ferrándiz C.
    Pediatr Dermatol; 2003; 20(2):113-8. PubMed ID: 12657005
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  • 3. Ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC): the clinical variation and prenatal diagnosis.
    Annerén G, Andersson T, Lindgren PG, Kjartansson S.
    Clin Genet; 1991 Oct; 40(4):257-62. PubMed ID: 1756598
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  • 4. Ectrodactyly, ectodermal dysplasia and clefting (EEC) syndrome.
    Glorio R, Haas R, Jaimovich L.
    J Eur Acad Dermatol Venereol; 2003 May; 17(3):356-8. PubMed ID: 12702090
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  • 7. Split hand and food deformity and the syndrome of ectrodactyly, ectodermal dysplasia, and clefting (EEC). A report of five patients.
    Schmidt R, Nitowsky HM.
    Hum Genet; 1977 Nov 02; 39(1):15-25. PubMed ID: 924443
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  • 9. A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting.
    Sorasio L, Biamino E, Garelli E, Ferrero GB, Silengo MC.
    Clin Exp Dermatol; 2009 Dec 02; 34(8):e726-8. PubMed ID: 19663851
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  • 10. EEC syndrome: report on 20 new patients, clinical and genetic considerations.
    Rodini ES, Richieri-Costa A.
    Am J Med Genet; 1990 Sep 02; 37(1):42-53. PubMed ID: 2240042
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  • 12. Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: five new mutations in the DNA-binding domain of the TP63 gene and genotype-phenotype correlation.
    Clements SE, Techanukul T, Coman D, Mellerio JE, McGrath JA.
    Br J Dermatol; 2010 Jan 02; 162(1):201-7. PubMed ID: 19903181
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  • 18. [Ectodermal dysplasia, ectrodactyly and clefting syndrome: ocular manifestations of this syndrome in a case report].
    Almeida SF, Solari HP.
    Arq Bras Oftalmol; 2007 Jan 02; 70(1):125-8. PubMed ID: 17505732
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  • 19. Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome: dominant inheritance and variable expression.
    Penchaszadeh VB, de Negrotti TC.
    J Med Genet; 1976 Aug 02; 13(4):281-4. PubMed ID: 957377
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