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Journal Abstract Search

360 related items for PubMed ID: 19451503

  • 1. Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entity.
    González-Enseñat MA, Vicente A, Poo P, Catalá V, Mar Pérez-Iribarne M, Fuster C, Geán E, Happle R.
    Arch Dermatol; 2009 May; 145(5):576-8. PubMed ID: 19451503
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  • 8. Mosaic tetrasomy 13q and phylloid hypomelanosis: a case report and review of the literature.
    Myers JN, Davis L, Sheehan D, Kulharya AS.
    Pediatr Dermatol; 2015 May; 32(2):263-6. PubMed ID: 24920397
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  • 9. Phylloid pattern of pigmentary disturbance in a case of complex mosaicism.
    Ribeiro Noce T, de Pina-Neto JM, Happle R.
    Am J Med Genet; 2001 Jan 15; 98(2):145-7. PubMed ID: 11223850
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  • 13. Patau syndrome with long survival in a case of unusual mosaic trisomy 13.
    Fogu G, Maserati E, Cambosu F, Moro MA, Poddie F, Soro G, Bandiera P, Serra G, Tusacciu G, Sanna G, Mazzarello V, Montella A.
    Eur J Med Genet; 2008 Jan 15; 51(4):303-14. PubMed ID: 18495567
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  • 16. Keratinocyte cytogenetics in 10 patients with pigmentary mosaicism: identification of one case of trisomy 20 mosaicism confined to keratinocytes.
    Taibjee SM, Hall D, Balderson D, Larkins S, Stubbs T, Moss C.
    Clin Exp Dermatol; 2009 Oct 15; 34(7):823-9. PubMed ID: 19438553
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  • 18. Sweat testing in hypomelanosis of Ito: divergent results reflecting genetic heterogeneity.
    Steijlen PM, Viëtor HE, Steensel MV, Happle R.
    Eur J Dermatol; 2000 Oct 15; 10(3):217-9. PubMed ID: 10725822
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  • 19. A case with mosaic partial duplication of 1q: prenatal and postmortem clinical and cytogenetic evaluations.
    Karaoguz MY, Biri A, Pala E, Kan D, Poyraz A, Kurdoglu M, Percin EF.
    Genet Couns; 2006 Oct 15; 17(2):197-204. PubMed ID: 16970038
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  • 20. Celiac disease, phylloid hypomelanosis and autoimmune thyroiditis: a case report.
    Tosun MS, Ertekin V.
    Turk J Pediatr; 2015 Oct 15; 57(6):639-641. PubMed ID: 27735809
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