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PUBMED FOR HANDHELDS

Journal Abstract Search


226 related items for PubMed ID: 8305327

  • 1. Rapp-Hodgkin syndrome and AEC syndrome: are they the same entity?
    Cambiaghi S, Tadini G, Barbareschi M, Menni S, Caputo R.
    Br J Dermatol; 1994 Jan; 130(1):97-101. PubMed ID: 8305327
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  • 2. Ectodermal dysplasia showing clinical overlap between AEC, Rapp-Hodgkin and CHAND syndromes.
    Sahin MT, Türel-Ermertcan A, Chan I, McGrath JA, Oztürkcan S.
    Clin Exp Dermatol; 2004 Sep; 29(5):486-8. PubMed ID: 15347331
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  • 3. Ectodermal dysplasias associated with clefting: significance of scalp dermatitis.
    Fosko SW, Stenn KS, Bolognia JL.
    J Am Acad Dermatol; 1992 Aug; 27(2 Pt 1):249-56. PubMed ID: 1341424
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  • 4. Scalp dermatitis, ectodermal dysplasia and cleft lip and palate: rapp-hodgkin or AEC syndrome.
    Rowan DM.
    Australas J Dermatol; 1996 May; 37(2):102-3. PubMed ID: 8687323
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  • 5. Skin symptoms in four ectodermal dysplasia syndromes including two case reports of Rapp-Hodgkin-Syndrome.
    Knaudt B, Volz T, Krug M, Burgdorf W, Röcken M, Berneburg M.
    Eur J Dermatol; 2012 May; 22(5):605-13. PubMed ID: 22759387
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  • 8. Mixed clefting type in Rapp-Hodgkin syndrome.
    Neilson DE, Brunger JW, Heeger S, Bamshad M, Robin NH.
    Am J Med Genet; 2002 Apr 01; 108(4):281-4. PubMed ID: 11920831
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  • 10. Rapp-Hodgkin and Hay-Wells ectodermal dysplasia syndromes represent a variable spectrum of the same genetic disorder.
    Clements SE, Techanukul T, Holden ST, Mellerio JE, Dorkins H, Escande F, McGrath JA.
    Br J Dermatol; 2010 Sep 01; 163(3):624-9. PubMed ID: 20491771
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  • 13. Facial clefting and oroauditory pathway manifestations in ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome.
    Cole P, Hatef DA, Kaufman Y, Magruder A, Bree A, Friedman E, Sindwani R, Hollier LH.
    Am J Med Genet A; 2009 Sep 01; 149A(9):1910-5. PubMed ID: 19697430
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  • 14. Craniofacial and anthropometric phenotype in ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (Hay-Wells syndrome) in a cohort of 17 patients.
    Sutton VR, Plunkett K, Dang DX, Lewis RA, Bree AF, Bacino CA.
    Am J Med Genet A; 2009 Sep 01; 149A(9):1916-21. PubMed ID: 19676059
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  • 16. A spectrum of TP63-related disorders with eight affected individuals in five unrelated families.
    Soğukpınar M, Utine GE, Boduroğlu K, Şimşek-Kiper PÖ.
    Eur J Med Genet; 2024 Apr 01; 68():104911. PubMed ID: 38281558
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  • 18. Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology.
    Clements SE, Techanukul T, Lai-Cheong JE, Mee JB, South AP, Pourreyron C, Burrows NP, Mellerio JE, McGrath JA.
    Br J Dermatol; 2012 Jul 01; 167(1):134-44. PubMed ID: 22329826
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  • 19. Severe skin erosions and scalp infections in AEC syndrome.
    Vanderhooft SL, Stephan MJ, Sybert VP.
    Pediatr Dermatol; 1993 Dec 01; 10(4):334-40. PubMed ID: 8302735
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  • 20. Ankyloblepharon-ectodermal dysplasia-clefting syndrome misdiagnosed as epidermolysis bullosa and congenital ichthyosiform erythroderma: Case report and review of published work.
    Zhang Z, Cheng R, Liang J, Lu Z, Wang Y, Li M, Yu H, Yao Z.
    J Dermatol; 2019 May 01; 46(5):422-425. PubMed ID: 30809829
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