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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

208 related items for PubMed ID: 11185738

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  • 5. Three Finnish incontinentia pigmenti (IP) families with recombinations with the IP loci at Xq28 and Xp11.
    Hydén-Granskog C, Salonen R, von Koskull H.
    Hum Genet; 1993 Mar; 91(2):185-9. PubMed ID: 8096494
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  • 8. [Incontinentia pigmenti in a male infant].
    Vehring KH, Kurlemann G, Traupe H, Bonsmann G, Gerding H, Möllmann S, Hamm H.
    Hautarzt; 1993 Nov; 44(11):726-30. PubMed ID: 8276592
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  • 12. Incontinentia pigmenti in male patients.
    Pacheco TR, Levy M, Collyer JC, de Parra NP, Parra CA, Garay M, Aprea G, Moreno S, Mancini AJ, Paller AS.
    J Am Acad Dermatol; 2006 Aug; 55(2):251-5. PubMed ID: 16844507
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  • 13. Unstable pre-mutation may explain mosaic disease expression of incontinentia pigmenti in males.
    Traupe H, Vehring KH.
    Am J Med Genet; 1994 Feb 15; 49(4):397-8. PubMed ID: 8160732
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  • 18. Skin lesion development in a mouse model of incontinentia pigmenti is triggered by NEMO deficiency in epidermal keratinocytes and requires TNF signaling.
    Nenci A, Huth M, Funteh A, Schmidt-Supprian M, Bloch W, Metzger D, Chambon P, Rajewsky K, Krieg T, Haase I, Pasparakis M.
    Hum Mol Genet; 2006 Feb 15; 15(4):531-42. PubMed ID: 16399796
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  • 20. [Incontinentia pigmenti. A rare disease with many symptoms].
    Holmström G, Bergendal B, Hallberg G, Marcus S, Hallén A, Dahl N.
    Lakartidningen; 2002 Mar 21; 99(12):1345-50. PubMed ID: 11998169
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