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Journal Abstract Search

232 related items for PubMed ID: 6837633

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  • 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
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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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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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  • 10. Scalp-ear-nipple syndrome: additional manifestations.
    Edwards MJ, McDonald D, Moore P, Rae J.
    Am J Med Genet; 1994 Apr 15; 50(3):247-50. PubMed ID: 8042668
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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 15; 20(1):197-202. PubMed ID: 2982262
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  • 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
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  • 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
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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
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