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Journal Abstract Search

350 related items for PubMed ID: 3868444

  • 21. [A family with the EEC syndrome (ectrodactily, ectodermal dysplasia clefting syndrome): clinical variability and genetic counseling].
    Gualandri V, Ronzoni MG, Montagnani A, Orsini GB.
    J Fr Ophtalmol; 1986; 9(12):855-7. PubMed ID: 3571845
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  • 30. De novo missense mutation, S541Y, in the p63 gene underlying Rapp-Hodgkin ectodermal dysplasia syndrome.
    Shotelersuk V, Janklat S, Siriwan P, Tongkobpetch S.
    Clin Exp Dermatol; 2005 May; 30(3):282-5. PubMed ID: 15807690
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  • 32. EEC syndrome: report on 20 new patients, clinical and genetic considerations.
    Rodini ES, Richieri-Costa A.
    Am J Med Genet; 1990 Sep; 37(1):42-53. PubMed ID: 2240042
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  • 34. A 19-year follow-up of a patient with type 3 ectrodactyly-ectodermal dysplasia-clefting syndrome who developed non-Hodgkin lymphoma.
    Balci S, Engiz O, Okten G, Sipahier M, Gursu G, Kandemir B.
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Sep; 108(3):e91-5. PubMed ID: 19716498
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  • 35. Ectrodactyly, ectodermal dysplasia, and cleft lip-palate (EEC) syndrome without clefting: a rare case report.
    Malvankar DD, Sacchidanand S, Mallikarjun M.
    Dermatol Online J; 2012 Feb 15; 18(2):5. PubMed ID: 22398226
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  • 37. Phenotypic variability in van der Woude syndrome.
    Lacombe D, Pedespan JM, Fontan D, Chateil JF, Verloes A.
    Genet Couns; 1995 Feb 15; 6(3):221-6. PubMed ID: 8588850
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