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Journal Abstract Search

154 related items for PubMed ID: 11102936

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  • 4. Mosaic trisomy 7 in a patient with pigmentary abnormalities.
    Verghese S, Newlin A, Miller M, Burton BK.
    Am J Med Genet; 1999 Dec 22; 87(5):371-4. PubMed ID: 10594873
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  • 5. 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 22; 34(7):823-9. PubMed ID: 19438553
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  • 6. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.
    Hartmann A, Hofmann UB, Hoehn H, Broecker EB, Hamm H.
    Pediatr Dermatol; 2004 Oct 22; 21(6):636-41. PubMed ID: 15575846
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  • 7. Clinical outcome and follow-up of the first reported case of Russell-Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7.
    Font-Montgomery E, Stone KM, Weaver DD, Vance GH, Das S, Thurston VC.
    Birth Defects Res A Clin Mol Teratol; 2005 Aug 22; 73(8):577-82. PubMed ID: 16007591
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  • 8. Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver-Russell syndrome.
    Flori E, Girodon E, Samama B, Becmeur F, Viville B, Girard-Lemaire F, Doray B, Schluth C, Marcellin L, Boehm N, Goossens M, Pingault V.
    Eur J Hum Genet; 2005 Sep 22; 13(9):1013-8. PubMed ID: 15915162
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  • 10. 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 22; 145(5):576-8. PubMed ID: 19451503
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  • 11. Mosaic trisomy 14 with hepatic involvement.
    Iglesias A, McCurdy LD, Glass IA, Cotter PD, Illueca M, Perenyi A, Sansaricq C.
    Ann Genet; 1997 May 22; 40(2):104-8. PubMed ID: 9259957
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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 May 22; 51(4):303-14. PubMed ID: 18495567
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  • 14. Delineation of a clinical syndrome caused by mosaic trisomy 15.
    Bühler EM, Bienz G, Straumann E, Bösch N.
    Am J Med Genet; 1996 Mar 15; 62(2):109-12. PubMed ID: 8882390
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  • 15. An unusual human mosaic for skin pigmentation.
    Stoll C, Alembik Y, Grosshans E, de Saint Martin A.
    Genet Couns; 2002 Mar 15; 13(3):281-7. PubMed ID: 12416635
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  • 16. Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies.
    Kulharya AS, Lovell CM, Flannery DB.
    Am J Med Genet; 2002 Dec 15; 113(4):367-70. PubMed ID: 12457409
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  • 17. Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3q.
    Portnoï MF, Boutchneï S, Bouscarat F, Morlier G, Nizard S, Dersarkissian H, Crickx B, Nouchy M, Taillemite JL, Belaich S.
    J Med Genet; 1999 Mar 15; 36(3):246-50. PubMed ID: 10204855
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  • 18. A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21.
    Hu J, Shekhter-Levin S, Shaw PH, Bay C, Kochmar S, Surti U.
    Cancer Genet Cytogenet; 2005 Jan 01; 156(1):62-7. PubMed ID: 15588858
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  • 19. [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 01; 130(11):1033-8. PubMed ID: 14724538
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  • 20. Blaschkolinear malformation syndrome in complex trisomy-7 mosaicism.
    Magenis E, Webb MJ, Spears B, Opitz JM.
    Am J Med Genet; 1999 Dec 22; 87(5):375-83. PubMed ID: 10594874
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