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Journal Abstract Search

159 related items for PubMed ID: 8882390

  • 1. 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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  • 2. Mosaic trisomy 9 syndrome with unusual phenotype.
    Kaminker CP, Daín L, Lamas MA, Sánchez JM.
    Am J Med Genet; 1985 Oct 15; 22(2):237-41. PubMed ID: 3931476
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  • 3. Trisomy 9 mosaicism syndrome. A case report and review of the literature.
    Tarani L, Colloridi F, Raguso G, Rizzuti A, Bruni L, Tozzi MC, Palermo D, Panero A, Vignetti P.
    Ann Genet; 1994 Oct 15; 37(1):14-20. PubMed ID: 8010707
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  • 5. Unique mosaicism of tetraploidy and trisomy 8: clinical, cytogenetic, and molecular findings in a live-born infant.
    Roberts HE, Saxe DF, Muralidharan K, Coleman KB, Zacharias JF, Fernhoff PM.
    Am J Med Genet; 1996 Mar 29; 62(3):243-6. PubMed ID: 8882781
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  • 6. Mosaic vs. nonmosaic trisomy 9: report of a liveborn infant evaluated by fluorescence in situ hybridization and review of the literature.
    Cantú ES, Eicher DJ, Pai GS, Donahue CJ, Harley RA.
    Am J Med Genet; 1996 Apr 24; 62(4):330-5. PubMed ID: 8723059
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  • 7. Clinical delineation of trisomy 9 syndrome.
    Katayama KP, Wilkinson EJ, Herrmann J, Glaspey JC, Agarwal AB, Roesler MR, Mattingly RF.
    Obstet Gynecol; 1980 Nov 24; 56(5):665-8. PubMed ID: 7432742
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  • 8. Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases.
    Reynolds JF, Daniel A, Kelly TE, Gollin SM, Stephan MJ, Carey J, Adkins WN, Webb MJ, Char F, Jimenez JF.
    Am J Med Genet; 1987 Jun 24; 27(2):257-74. PubMed ID: 3605212
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  • 9. 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 Jun 24; 21(6):636-41. PubMed ID: 15575846
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  • 10. First report of mosaic trisomy 12 in a liveborn individual.
    Patil SR, Bosch EP, Hanson JW.
    Am J Med Genet; 1983 Mar 24; 14(3):453-60. PubMed ID: 6859097
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  • 11. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
    Crowe CA, Schwartz S, Black CJ, Jaswaney V.
    Am J Med Genet; 1997 Sep 05; 71(4):406-13. PubMed ID: 9286446
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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 Sep 05; 51(4):303-14. PubMed ID: 18495567
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  • 16. Trisomy 14 mosaicism syndrome.
    Lipson MH.
    Am J Med Genet; 1987 Mar 05; 26(3):541-4. PubMed ID: 3565467
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  • 17. Prenatal diagnosis of trisomy 6 mosaicism.
    Destree A, Fourneau C, Dugauquier C, Rombout S, Sartenaer D, Gillerot Y.
    Prenat Diagn; 2005 May 05; 25(5):354-7. PubMed ID: 15906424
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  • 20. Unilateral microtia in an infant with trisomy 18 mosaicism.
    Giannatou E, Leze H, Katana A, Kolialexi A, Mavrou A, Kanavakis E, Kitsiou-Tzeli S.
    Genet Couns; 2009 May 05; 20(2):181-7. PubMed ID: 19650416
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