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Journal Abstract Search

409 related items for PubMed ID: 7504881

  • 1. Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: a distinct syndrome.
    Ladda RL, Zonana J, Ramer JC, Mascari MJ, Rogan PK.
    Am J Med Genet; 1993 Sep 15; 47(4):550-5. PubMed ID: 7504881
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  • 2. [Ectrodactyly, ectodermal dysplasia, and cleft lip and palate: an hereditary syndrome with an autosomal dominant mode of inheritance (author's transl)].
    Pfeiffer RA, Verbeck C.
    Z Kinderheilkd; 1973 Oct 01; 115(3):235-44. PubMed ID: 4801123
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  • 3. Counseling dilemmas in EEC syndrome.
    Tekin M, Ohle C, Johnson DE, Christmas JT, Bodurtha J.
    Genet Couns; 2000 Oct 01; 11(1):19-24. PubMed ID: 10756423
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  • 4. [Familial split hand and foot, cleft lip and palate, ectodermal dysplasia syndrome].
    Szappanos L, Czeizel E, Szepesi K.
    Orv Hetil; 1984 Mar 11; 125(11):633-8. PubMed ID: 6700970
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  • 6. Autosomal recessive ectodermal dysplasia, cleft lip/palate, mental retardation, and syndactyly: the Zlotogora-Ogur syndrome.
    Rodini ES, Richieri-Costa A.
    Am J Med Genet; 1990 Aug 11; 36(4):473-6. PubMed ID: 2167611
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  • 7. Association of syndactyly, ectodermal dysplasia, and cleft lip and palate: report of two sibs from Turkey.
    Oğur G, Yüksel M.
    J Med Genet; 1988 Jan 11; 25(1):37-40. PubMed ID: 2832607
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  • 8. [Ectrodactyly, ectodermal dysplasia, cleft lip and palate syndrome (EEC syndrome)].
    Ostorharics-Horváth G, Lázár I.
    Orv Hetil; 1989 Oct 08; 130(41):2211-2. PubMed ID: 2812754
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  • 12. Short stature, mental retardation, eye anomalies, and cleft lip/palate.
    Richieri-Costa A, Guion-Almeida ML.
    Am J Med Genet; 1992 Feb 15; 42(4):449-52. PubMed ID: 1609826
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  • 14. AEC syndrome: further evidence of a common genetic etiology with Rapp-Hodgkin syndrome.
    Sorasio L, Ferrero GB, Garelli E, Brunello G, Martano C, Carando A, Belligni E, Dianzani I, Cirillo Silengo M.
    Eur J Med Genet; 2006 Feb 15; 49(6):520-2. PubMed ID: 16824815
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  • 17. Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her child.
    Moerman P, Fryns JP.
    Am J Med Genet; 1996 Jun 14; 63(3):479-81. PubMed ID: 8737656
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  • 20. Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.
    Koillinen H, Wong FK, Rautio J, Ollikainen V, Karsten A, Larson O, Teh BT, Huggare J, Lahermo P, Larsson C, Kere J.
    Eur J Hum Genet; 2001 Oct 14; 9(10):747-52. PubMed ID: 11781685
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