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Journal Abstract Search

126 related items for PubMed ID: 7929942

  • 1. Natural history of the Naegeli-Franceschetti-Jadassohn syndrome.
    Papini M.
    J Am Acad Dermatol; 1994 Nov; 31(5 Pt 1):830. PubMed ID: 7929942
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  • 4. Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: intrafamilial overlap of phenotypes in patients with the same KRT14 frameshift variant.
    Burger B, Spoerri I, Imahorn E, Wariwoda H, Leeb T, Itin PH.
    Br J Dermatol; 2019 Oct; 181(4):864-866. PubMed ID: 30968399
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  • 5. Refined mapping of Naegeli-Franceschetti- Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genes.
    Sprecher E, Itin P, Whittock NV, McGrath JA, Meyer R, DiGiovanna JJ, Bale SJ, Uitto J, Richard G.
    J Invest Dermatol; 2002 Sep; 119(3):692-8. PubMed ID: 12230514
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  • 8. Reticulate pigmentary dermatosis associated with hypohydrosis and short stature: a variant of Naegeli-Franceschetti-Jadassohn syndrome?
    Kudo Y, Fujiwara S, Takayasu S, Ooki H, Ogawa A.
    Int J Dermatol; 1995 Jan; 34(1):30-1. PubMed ID: 7896482
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  • 9. Prenatal and postnatal growth retardation, microcephaly, developmental delay, and pigmentation abnormalities: Naegeli syndrome, dyskeratosis congenita, poikiloderma Clericuzio type, or separate entity?
    Belligni EF, Dokal I, Hennekam RC.
    Eur J Med Genet; 2011 Jan; 54(3):231-5. PubMed ID: 21252004
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  • 10. [Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis. Two allelic ectodermal dysplasias related to mutations of dominant gene coding for keratin 14].
    Dereure O.
    Ann Dermatol Venereol; 2007 Jan; 134(6-7):595. PubMed ID: 17657198
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  • 14. Connexin disorders of the skin.
    Richard G.
    Adv Dermatol; 2001 Jan; 17():243-77. PubMed ID: 11758118
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  • 15. Anhidrotic (or hypohidrotic) ectodermal dysplasis.
    Martin-Pascual A, De Unamuno P, Aparicio M, Herreros V.
    Dermatologica; 1977 Jan; 154(4):235-43. PubMed ID: 140825
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  • 16. Variant of odontoonychodermal dysplasia?
    Arnold WP, Merkx MA, Steijlen PM.
    Am J Med Genet; 1995 Nov 06; 59(2):242-4. PubMed ID: 8588594
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  • 17. Hypohidrotic ectodermal dysplasia (Christ-Siemans-Touraine syndrome) in siblings.
    Nathan V.
    West Indian Med J; 1984 Mar 06; 33(1):55-8. PubMed ID: 6730467
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  • 18. [Autosomal recessive ectodermal dysplasia--a special nosologic entity? (author's transl)].
    Lelis J.
    Dermatol Monatsschr; 1979 Aug 06; 165(8):587-92. PubMed ID: 159839
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  • 19. [Verruciform palmoplantar keratoderma as a characteristic marker of hidrotic ectodermal dysplasia of the Clouston type].
    Koch P, Foss P, Baum HP, Zaun H.
    Hautarzt; 1995 Apr 06; 46(4):272-5. PubMed ID: 7790195
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  • 20. Oral findings of Clouston's syndrome (hidrotic ectodermal dysplasia).
    George DI, Escobar VH.
    Oral Surg Oral Med Oral Pathol; 1984 Mar 06; 57(3):258-62. PubMed ID: 6584816
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