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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

150 related items for PubMed ID: 1010929

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  • 2. Three variations of hairlessness associated with albinism in the laboratory rat.
    Ferguson FG, Irving GW, Stedham MA.
    Lab Anim Sci; 1979 Aug; 29(4):459-64. PubMed ID: 513614
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  • 3. Shorn (shn): a new mutation causing hypotrichosis in the Norway rat.
    Moemeka AN, Hildebrandt AL, Radaskiewicz P, King TR.
    J Hered; 1998 Aug; 89(3):257-60. PubMed ID: 9656468
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  • 10. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis.
    Lefevre P, Rochat A, Bodemer C, Vabres P, Barrandon Y, de Prost Y, Garner C, Hovnanian A.
    Eur J Hum Genet; 2000 Apr; 8(4):273-9. PubMed ID: 10854110
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  • 11. Desmoglein 4 mutations underlie localized autosomal recessive hypotrichosis in humans, mice, and rats.
    Bazzi H, Martinez-Mir A, Kljuic A, Christiano AM.
    J Investig Dermatol Symp Proc; 2005 Dec; 10(3):222-4. PubMed ID: 16382669
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  • 13. A spontaneous mutation in the desmoglein 4 gene underlies hypotrichosis in a new lanceolate hair rat model.
    Meyer B, Bazzi H, Zidek V, Musilova A, Pravenec M, Kurtz TW, Nurnberg P, Christiano AM.
    Differentiation; 2004 Dec; 72(9-10):541-7. PubMed ID: 15617564
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  • 19. A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities.
    Farkas K, Nagy N, Kinyó A, Kemény L, Széll M.
    Arch Dermatol Res; 2012 Oct; 304(8):679-81. PubMed ID: 22584530
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