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Journal Abstract Search

338 related items for PubMed ID: 1456284

  • 1. Autosomal recessive cleft lip/palate, ectodermal dysplasia, and minor acral anomalies: report of a Brazilian family.
    Richieri-Costa A, Guion-Almeida ML, Freire-Maia N, Pinheiro M.
    Am J Med Genet; 1992 Sep 15; 44(2):158-62. PubMed ID: 1456284
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  • 3. EEC syndrome: report on 20 new patients, clinical and genetic considerations.
    Rodini ES, Richieri-Costa A.
    Am J Med Genet; 1990 Sep 15; 37(1):42-53. PubMed ID: 2240042
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  • 4. Cleft lip/palate-oligodontia-syndactyly-hair alterations, a new syndrome: review of the conditions combining ectodermal dysplasia and cleft lip/palate.
    Martínez B, Monasterio L, Pinheiro M, Freire-Maia N.
    Am J Med Genet; 1987 May 15; 27(1):23-31. PubMed ID: 3037904
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  • 5. Rapp-Hodgkin syndrome: report of a Brazilian family.
    Rodini EO, Freitas JA, Richieri-Costa A.
    Am J Med Genet; 1990 Aug 15; 36(4):463-6. PubMed ID: 2389804
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  • 8. 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 15; 33(2):190-3. PubMed ID: 2764029
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  • 9. Autosomal recessive blepharoptosis, cleft lip/palate, dental anomalies, and ectrodactyly.
    Rodini ES, Richieri-Costa A.
    Am J Med Genet; 1992 Feb 01; 42(3):340-2. PubMed ID: 1536175
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  • 10. [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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  • 11. 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 01; 25(1):37-40. PubMed ID: 2832607
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  • 15. Odontoonychodysplasia with alopecia: a new pure ectodermal dysplasia with probable autosomal recessive inheritance.
    Pinheiro M, Freire-Maia N, Gollop TR.
    Am J Med Genet; 1985 Jan 01; 20(1):197-202. PubMed ID: 2982262
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  • 16. A de novo heterozygous point mutation in the p63 gene causing the syndrome of ectrodactyly, ectodermal dysplasia and facial clefting.
    Pozo G, Canún S, Kofman-Alfaro S, Zenteno JC.
    Br J Dermatol; 2004 Oct 01; 151(4):930-2. PubMed ID: 15491445
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  • 17. Marden-Walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consanguineous parents.
    van den Ende JJ, van Bever Y, Rodini ES, Richieri-Costa A.
    Am J Med Genet; 1992 Feb 15; 42(4):467-9. PubMed ID: 1609830
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  • 18. Genitourinary anomalies are a component manifestation in the ectodermal dysplasia, ectrodactyly, cleft lip/palate (EEC) syndrome.
    Rollnick BR, Hoo JJ.
    Am J Med Genet; 1988 Jan 15; 29(1):131-6. PubMed ID: 3278611
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  • 19. Ectrodactary, ectodermal dysplasia, and cleft lip-palate syndrome.
    Choong YY, Norazlina B.
    Med J Malaysia; 2001 Mar 15; 56(1):88-91. PubMed ID: 11503303
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  • 20. Aarskog syndrome in a Brazilian boy born to consanguineous parents.
    Guion-Almeida ML, Richieri-Costa A.
    Am J Med Genet; 1992 Jul 15; 43(5):808-10. PubMed ID: 1642267
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