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Journal Abstract Search

149 related items for PubMed ID: 8588594

  • 21. Mental retardation, hypotrichosis and syndactyly: a new entity?
    Lopes VL, Marques-De-Faria AP.
    Genet Couns; 1996; 7(1):47-51. PubMed ID: 8652088
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  • 23. [Contribution to the problem of ectodermal dysplasia in children].
    Remiszewski A.
    Pediatr Pol; 1983 Mar; 58(3):299-305. PubMed ID: 6312402
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  • 25. Schöpf-Schulz-Passarge syndrome with pili torti: A new association?
    SZEPETIUK G, VANHOOTEGHEM O, MULLER G, STENE JJ, NIKKELS AF.
    Eur J Dermatol; 2009 Mar; 19(5):517-8. PubMed ID: 19527991
    [No Abstract] [Full Text] [Related]

  • 26. Anhidrotic (or hypohidrotic) ectodermal dysplasis.
    Martin-Pascual A, De Unamuno P, Aparicio M, Herreros V.
    Dermatologica; 1977 Mar; 154(4):235-43. PubMed ID: 140825
    [No Abstract] [Full Text] [Related]

  • 27. Trichodental dysplasia: a rare syndrome with distinct dental findings.
    Montalvan E, Mazzone C, Tofsky N, Mupparapu M.
    Pediatr Dent; 2006 Mar; 28(4):345-9. PubMed ID: 16903444
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  • 29. Further delineation of the odonto-onycho-dermal dysplasia syndrome.
    Mégarbané H, Haddad M, Delague V, Renoux J, Boehm N, Mégarbané A.
    Am J Med Genet A; 2004 Aug 30; 129A(2):193-7. PubMed ID: 15316967
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  • 32. Ectodermal dysplasia--a new variant?
    Bartalos M, Saraçli T.
    J Genet Hum; 1968 Jan 30; 16(3):49-56. PubMed ID: 5710712
    [No Abstract] [Full Text] [Related]

  • 33. Congenital atrichia, palmoplantar hyperkeratosis, mental retardation, and early loss of teeth in four siblings: a new syndrome?
    Steijlen PM, Neumann HA, der Kinderen DJ, Smeets DF, van der Kerkhof PC, Happle R.
    J Am Acad Dermatol; 1994 May 30; 30(5 Pt 2):893-8. PubMed ID: 8169270
    [Abstract] [Full Text] [Related]

  • 34. JAAD Grand Rounds quiz. Palmoplantar keratoderma, hypodontia, hypotrichosis, nail dystrophy, and multiple eyelid cysts.
    DiGiorgio CM, Bohlke AK, Oswald BJ, Wang AR, Boh EE.
    J Am Acad Dermatol; 2011 Nov 30; 65(5):1066-9. PubMed ID: 22000878
    [No Abstract] [Full Text] [Related]

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  • 36. Rapp-Hodgkin syndrome with palmoplantar keratoderma, glossy tongue, congenital absence of lingual frenum and of sublingual caruncles: newly recognized findings.
    Kantaputra PN, Pruksachatkunakorn C, Vanittanakom P.
    Am J Med Genet; 1998 Oct 12; 79(5):343-6. PubMed ID: 9779799
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  • 38. A severe case of pachyonychia congenita type I due to a novel proline mutation in keratin 6a.
    García-Rio I, Peñas PF, García-Díez A, McLean WH, Smith FJ.
    Br J Dermatol; 2005 Apr 12; 152(4):800-2. PubMed ID: 15840119
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  • 40. Ectodermal dysplasia syndrome with eyebrow alopecia, ptosis, strabismus, nystagmus, joint laxity, cerebellar ataxia, and osteopenia.
    Zannolli R, Inchingolo G, Serracca L, Miracco C, De Santi MM, Malandrini A, Biagioli M, Perotti R, Baldi C, Nuti D, Polito E, Gonnelli S.
    Am J Med Genet; 2002 Nov 15; 113(1):111-3. PubMed ID: 12400077
    [No Abstract] [Full Text] [Related]

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