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Journal Abstract Search


265 related items for PubMed ID: 8882781

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Homozygous alpha-thalassemia with trisomy 7 mosaicism in a live-born infant.
    Quintero-Rivera F, Abreu-E-Lima P, Zhang IH, Parast MM.
    Pediatr Hematol Oncol; 2009 Sep 29; 26(6):426-31. PubMed ID: 19657992
    [Abstract] [Full Text] [Related]

  • 3. "Mosaic trachea" in a child with trisomy 9 mosaicism.
    Gniady JP, Isaacson G, Ladda RL.
    Int J Pediatr Otorhinolaryngol; 2010 Oct 29; 74(10):1193-5. PubMed ID: 20727599
    [Abstract] [Full Text] [Related]

  • 4. Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18?
    Shashi V, Golden WL, von Kap-Herr C, Wilson WG.
    Am J Med Genet; 1996 Mar 01; 62(1):38-41. PubMed ID: 8779322
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Trisomy 9 mosaicism in a girl with multiple malformations.
    Diaz-Mares L, Molina B, Carnevale A.
    Ann Genet; 1990 Apr 24; 33(3):165-8. PubMed ID: 2288462
    [Abstract] [Full Text] [Related]

  • 7. Tetrasomy 5p mosaicism due to an extra i(5p) in a severely affected girl.
    Lorda-Sánchez I, Villa A, Urioste M, Bernal E, Jaso E, García A, Martínez-Frías ML.
    Am J Med Genet; 1997 Feb 11; 68(4):481-4. PubMed ID: 9021026
    [Abstract] [Full Text] [Related]

  • 8. Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype.
    Wieczorek D, Prott EC, Robinson WP, Passarge E, Gillessen-Kaesbach G.
    Prenat Diagn; 2003 Feb 11; 23(2):128-33. PubMed ID: 12575019
    [Abstract] [Full Text] [Related]

  • 9. Secondary trisomy or mosaic "tetrasomy" 8p.
    Robinow M, Haney N, Chen H, Sorauf T, Van Dyke DL, Babu VR, Powell S, Maliszewski W, Guerin S, Landers JW.
    Am J Med Genet; 1989 Mar 11; 32(3):320-4. PubMed ID: 2729351
    [Abstract] [Full Text] [Related]

  • 10. Mosaic tetrasomy 15q25-->qter in a newborn infant with multiple anomalies.
    Van den Enden A, Verschraegen-Spae MR, Van Roy N, Decaluwe W, De Praeter C, Speleman F.
    Am J Med Genet; 1996 Jun 14; 63(3):482-5. PubMed ID: 8737657
    [Abstract] [Full Text] [Related]

  • 11. Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant.
    Milunsky JM, Wyandt HE, Huang XL, Kang XZ, Elias ER, Milunsky A.
    Am J Med Genet; 1996 Jan 22; 61(3):269-73. PubMed ID: 8741873
    [Abstract] [Full Text] [Related]

  • 12. Tetraploidy: a report of three live-born infants.
    Scarbrough PR, Hersh J, Kukolich MK, Carroll AJ, Finley SC, Hochberger R, Wilkerson S, Yen FF, Althaus BW.
    Am J Med Genet; 1984 Sep 22; 19(1):29-37. PubMed ID: 6496571
    [Abstract] [Full Text] [Related]

  • 13. Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies.
    Genuardi M, Tozzi C, Pomponi MG, Stagni ML, Della Monica M, Scarano G, Calvieri F, Torrisi L, Neri G.
    Eur J Hum Genet; 1999 Sep 22; 7(4):421-6. PubMed ID: 10352932
    [Abstract] [Full Text] [Related]

  • 14. Variable clinical expression of mosaic trisomy 16 in the newborn infant.
    Devi AS, Velinov M, Kamath MV, Eisenfeld L, Neu R, Ciarleglio L, Greenstein R, Benn P.
    Am J Med Genet; 1993 Aug 15; 47(2):294-8. PubMed ID: 8213923
    [Abstract] [Full Text] [Related]

  • 15. MCA/MR syndrome in a female infant with tetraploidy mosaicism: review of the human polyploid phenotype.
    Wilson GN, Vekemans MJ, Kaplan P.
    Am J Med Genet; 1988 Aug 15; 30(4):953-61. PubMed ID: 3055989
    [Abstract] [Full Text] [Related]

  • 16. Duplication 2p and monosomy 8p in mosaicism: clinical, molecular cytogenetic and molecular markers of a unique case.
    Martínez A, Ramos S, González-del Angel A, Alcántara MA, Molina B, Carnevale A.
    Rev Invest Clin; 2007 Aug 15; 59(6):444-8. PubMed ID: 18402336
    [Abstract] [Full Text] [Related]

  • 17. 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 Aug 15; 21(6):636-41. PubMed ID: 15575846
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.
    Leichtman LG, Zackowski JL, Storto PD, Newlin A.
    Am J Med Genet; 1996 Jun 14; 63(3):434-7. PubMed ID: 8737648
    [Abstract] [Full Text] [Related]

  • 20. Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations.
    Wilson WG, Shires MA, Willson KA, Wyandt HE, Harris LM, Kelly TE.
    Am J Med Genet; 1983 Sep 14; 16(1):131-6. PubMed ID: 6638063
    [Abstract] [Full Text] [Related]


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