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Journal Abstract Search

155 related items for PubMed ID: 23095783

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  • 2. Phylloid hypomelanosis is closely related to mosaic trisomy 13.
    Happle R.
    Eur J Dermatol; 2000; 10(7):511-2. PubMed ID: 11056419
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  • 3. 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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  • 5. 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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  • 7. [Phylloid hypomelanosis and mosaic trisomy 13: a new etiologically defined neurocutaneous syndrome].
    Happle R.
    Hautarzt; 2001 Jan 15; 52(1):3-5. PubMed ID: 11220235
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  • 9. [Hypomelanosis of Ito in a girl with Trisomy 13 mosaicism: a cytogenetic study].
    Ronger S, Till M, Kanitakis J, Balme B, Thomas L.
    Ann Dermatol Venereol; 2003 Nov 15; 130(11):1033-8. PubMed ID: 14724538
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  • 11. Phylloid pigmentary pattern with mosaic trisomy 13.
    Horn D, Rommeck M, Sommer D, Körner H.
    Pediatr Dermatol; 1997 Nov 15; 14(4):278-80. PubMed ID: 9263307
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  • 12. The link between hidradenitis suppurativa and phylloid hypomelanosis in partial trisomy-13 mosaicism: New evidences and further genetic/pathogenetic insights.
    Forconi R, Bigoni S, Pacetti L, Host C, Schettini N, Zedde P, Buldrini B, Ferlini A, Bettoli V.
    Pediatr Dermatol; 2021 May 15; 38(3):637-639. PubMed ID: 33715178
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  • 13. Phylloid hypermelanosis and melanocytic nevi with aggregated and disfigured melanosomes: causal relationship between phylloid pigment distribution and chromosome 13 abnormalities.
    Oiso N, Tsuruta D, Imanishi H, Sayasa H, Narita T, Kobayashi H, Ikegami H, Kawada A.
    Dermatology; 2010 May 15; 220(2):169-72. PubMed ID: 20110628
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  • 17. 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 May 15; 51(4):303-14. PubMed ID: 18495567
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