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Journal Abstract Search

361 related items for PubMed ID: 3037904

  • 21. Syndactyly, ectodermal dysplasia, and cleft lip/palate.
    Zlotogora J.
    J Med Genet; 1994 Dec; 31(12):957-9. PubMed ID: 7891379
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  • 23. [Ectodactylia-ectodermal dysplasia, cleft lip, jaw and palate syndrome (EEC syndrome). Association with van der Woude syndrome?].
    Haensch R, Küster W, Hammerstein W.
    Dtsch Z Mund Kiefer Gesichtschir; 1985 Dec; 9(3):225-6. PubMed ID: 3868444
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  • 24. The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition.
    Hay RJ, Wells RS.
    Br J Dermatol; 1976 Mar; 94(3):277-89. PubMed ID: 946410
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  • 29. A case of the Freire-Maia Odontotrichomelic syndrome: nosology with EEC syndrome.
    Pavone L, Rizzo R, Tiné A, Micali G, Sorge G, Neri G.
    Am J Med Genet; 1989 Jun; 33(2):190-3. PubMed ID: 2764029
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  • 30. Tooth abnormalities and soft tissue alterations in patients with G/BBB syndrome.
    da Silva Dalben G, Richieri-Costa A, de Assis Taveira LA.
    Oral Dis; 2008 Nov; 14(8):747-53. PubMed ID: 18627501
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  • 31. [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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  • 32. [Association of ectodermal dysplasia, ectrodactyly and cleft lip-palate: the EEC syndrome].
    Romagnoli G, Zunin C.
    Pathologica; 1974 Oct 01; 66(953-954):95-103. PubMed ID: 4371344
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  • 33. Limb pterygium syndromes: a review and report of eleven patients.
    Hall JG, Reed SD, Rosenbaum KN, Gershanik J, Chen H, Wilson KM.
    Am J Med Genet; 1982 Aug 01; 12(4):377-409. PubMed ID: 7124793
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  • 34. Cardio-facio-cutaneous (CFC) syndrome: report of a new patient.
    Chrzanowska K, Fryns JP, Van den Berghe H.
    Am J Med Genet; 1989 Aug 01; 33(4):471-3. PubMed ID: 2596505
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  • 40. Ectodermal dysplasia, cleft lip/palate, and severe cutaneous and osseous syndactyly in a mentally retarded girl: a new multiple malformation syndrome.
    Freihofer HP, Walji S, Brunner HG.
    Am J Med Genet; 1997 Jun 13; 70(3):211-5. PubMed ID: 9188655
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