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Journal Abstract Search

232 related items for PubMed ID: 6837633

  • 1. Brief clinical report: new, autosomal dominant form of ectodermal dysplasia.
    Tuffli GA, Laxova R.
    Am J Med Genet; 1983 Feb; 14(2):381-4. PubMed ID: 6837633
    [Abstract] [Full Text] [Related]

  • 2. Family with autosomal dominant hidrotic ectodermal dysplasia: a previously unrecognised syndrome?
    Christianson AL, Fourie S.
    Am J Med Genet; 1996 Jun 28; 63(4):549-53. PubMed ID: 8826433
    [Abstract] [Full Text] [Related]

  • 3.
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  • 4. Pilodentoungulardysplasia with microcephaly: a new ectodermal dysplasia/malformation syndrome.
    Tajara EH, Pinheiro M, Freire-Maia N.
    Am J Med Genet; 1987 Jan 28; 26(1):153-6. PubMed ID: 3812555
    [Abstract] [Full Text] [Related]

  • 5. Odontoonychodermal dysplasia: a previously apparently undescribed ectodermal dysplasia.
    Fadhil M, Ghabra TA, Deeb M, Der Kaloustian VM.
    Am J Med Genet; 1983 Feb 28; 14(2):335-46. PubMed ID: 6837628
    [Abstract] [Full Text] [Related]

  • 6. Keratin 17 mutation in pachyonychia congenita type 2 patient with early onset steatocystoma multiplex and Hutchinson-like tooth deformity.
    Oh SW, Kim MY, Lee JS, Kim SC.
    J Dermatol; 2006 Mar 28; 33(3):161-4. PubMed ID: 16620218
    [Abstract] [Full Text] [Related]

  • 7. Ectodermal dysplasia with corkscrew hairs: observation of probable autosomal dominant tricho-odonto-onychodysplasia with syndactyly.
    Trüeb R, Burg G, Bottani A, Schinzel A.
    J Am Acad Dermatol; 1994 Feb 28; 30(2 Pt 1):289-90. PubMed ID: 8141890
    [No Abstract] [Full Text] [Related]

  • 8. Polydactyly with ectodermal defect, osteopenia, and mental delay.
    Zannolli R, Buoni S, Viviano M, Macucci F, D'Ambrosio A, Livi W, Mazzei MA, Mazzei F, Sacco P, Volterrani L, Vonella G, Orsi A, Zappella M, Hayek J.
    J Child Neurol; 2008 Jun 28; 23(6):683-9. PubMed ID: 18182642
    [Abstract] [Full Text] [Related]

  • 9. A previously undescribed ectodermal dysplasia of the tricho-odonto-onychial subgroup in a family.
    Tsakalakos N, Jordaan FH, Taljaard JJ, Hough SF.
    Arch Dermatol; 1986 Sep 28; 122(9):1047-53. PubMed ID: 3740884
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  • 11. 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 28; 20(1):197-202. PubMed ID: 2982262
    [Abstract] [Full Text] [Related]

  • 12. Hereditary hypodontia and onychorrhexis of the fingernails and toenail koilonychia: Witkop's tooth-and nail syndrome.
    Zabawski EJ, Cohen JB.
    Dermatol Online J; 1999 May 28; 5(1):3. PubMed ID: 10673446
    [Abstract] [Full Text] [Related]

  • 13. [Basan's syndrome: dominant autosomal hypohidrotic ectodermal dysplasia].
    Hernando I, Benavides A, Plasencia A, Visus EP, Bousoño C, Fernández Toral J.
    An Esp Pediatr; 1988 Apr 28; 28(4):359-60. PubMed ID: 3400948
    [No Abstract] [Full Text] [Related]

  • 14. ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia.
    Propping P, Zerres K.
    Am J Med Genet; 1993 Mar 01; 45(5):642-8. PubMed ID: 8456838
    [Abstract] [Full Text] [Related]

  • 15. A new autosomal dominant syndrome of hypohidrotic ectodermal dysplasia and unusual facies.
    Bocian M, Rimoin DL.
    Birth Defects Orig Artic Ser; 1979 Mar 01; 15(5B):239-51. PubMed ID: 526580
    [No Abstract] [Full Text] [Related]

  • 16. The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition.
    Hay RJ, Wells RS.
    Br J Dermatol; 1976 Mar 01; 94(3):277-89. PubMed ID: 946410
    [Abstract] [Full Text] [Related]

  • 17. R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy.
    Valenzise M, Arrigo T, De Luca F, Privitera A, Frigiola A, Carando A, Garelli E, Silengo M.
    Eur J Med Genet; 2008 Mar 01; 51(5):497-500. PubMed ID: 18603493
    [Abstract] [Full Text] [Related]

  • 18. A rare case of tooth-nail syndrome.
    Mielnik-Błaszczak M, Tomankiewicz M.
    Ann Univ Mariae Curie Sklodowska Med; 2003 Mar 01; 58(2):306-10. PubMed ID: 15323210
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  • 19. ADULT ectodermal dysplasia syndrome resulting from the missense mutation R298Q in the p63 gene.
    Chan I, Harper JI, Mellerio JE, McGrath JA.
    Clin Exp Dermatol; 2004 Nov 01; 29(6):669-72. PubMed ID: 15550149
    [Abstract] [Full Text] [Related]

  • 20. Natal teeth and steatocystoma multiplex complicated by hidradenitis suppurativa. A new syndrome.
    McDonald RM, Reed WB.
    Arch Dermatol; 1976 Aug 01; 112(8):1132-4. PubMed ID: 988984
    [Abstract] [Full Text] [Related]

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