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Journal Abstract Search

527 related items for PubMed ID: 8779322

  • 1. 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]

  • 2. 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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  • 3. 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
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  • 4. 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
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  • 6. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
    Lorentz CP, Jalal SM, Thompson DM, Babovic-Vuksanovic D.
    Am J Med Genet; 2002 Jul 22; 111(1):61-7. PubMed ID: 12124737
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  • 8. 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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  • 9. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
    Schimmenti LA, Higgins RR, Mendelsohn NJ, Casey TM, Steinberger J, Mammel MC, Wiesner GL.
    Am J Med Genet; 1995 May 22; 57(1):52-6. PubMed ID: 7645598
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  • 10. Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies.
    Ergun MA, Balci S, Konaç E, Kan D, Menevşe S, Bartsch O.
    Turk J Pediatr; 2004 May 22; 46(4):384-7. PubMed ID: 15641279
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  • 11. Constitutional partial 1q trisomy mosaicism and Wilms tumor.
    Mark HF, Wyandt H, Pan A, Milunsky JM.
    Cancer Genet Cytogenet; 2005 Oct 15; 162(2):166-71. PubMed ID: 16213366
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  • 12. 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. 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 Sep 05; 37(1):14-20. PubMed ID: 8010707
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  • 14. A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome.
    Lee JH, Cho HS, Lee ES, Jung BC.
    Korean J Lab Med; 2010 Jun 05; 30(3):312-7. PubMed ID: 20603594
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  • 15. Trisomy 8 mosaicism syndrome.
    Fineman RM, Ablow RC, Howard RO, Albright J, Breg WR.
    Pediatrics; 1975 Nov 05; 56(5):762-7. PubMed ID: 1196733
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  • 17. 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
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  • 18. Trisomy 9: review and report of two new cases.
    Arnold GL, Kirby RS, Stern TP, Sawyer JR.
    Am J Med Genet; 1995 Apr 10; 56(3):252-7. PubMed ID: 7778584
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  • 19. Trisomy 9 mosaicism: another etiology for the manifestations of Goldenhar syndrome.
    Wilson GN, Barr M.
    J Craniofac Genet Dev Biol; 1983 Apr 10; 3(4):313-6. PubMed ID: 6662905
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