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Journal Abstract Search

268 related items for PubMed ID: 7778584

  • 1.
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  • 2. Atypical manifestations of two cases of trisomy 9 syndrome: rethinking development delay.
    Saneto RP, Applegate KE, Frankel DG.
    Am J Med Genet; 1998 Oct 30; 80(1):42-5. PubMed ID: 9800910
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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 30; 37(1):14-20. PubMed ID: 8010707
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  • 4. 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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  • 5. Trisomy 16 and trisomy 16 Mosaicism: a review.
    Benn P.
    Am J Med Genet; 1998 Sep 01; 79(2):121-33. PubMed ID: 9741470
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  • 6. Trisomy 20 mosaicism and nonmosaic trisomy 20: a report of 2 cases.
    Joó JG, Beke A, Tóth-Pál E, Hargitai B, Szigeti Z, Papp C, Papp Z.
    J Reprod Med; 2006 Mar 01; 51(3):209-12. PubMed ID: 16674019
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  • 7. 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 01; 32(3):320-4. PubMed ID: 2729351
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  • 9. Mosaic trisomy 9 syndrome with unusual phenotype.
    Kaminker CP, Daín L, Lamas MA, Sánchez JM.
    Am J Med Genet; 1985 Oct 01; 22(2):237-41. PubMed ID: 3931476
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  • 11. Clinical and molecular studies in full trisomy 22: further delineation of the phenotype and review of the literature.
    Bacino CA, Schreck R, Fischel-Ghodsian N, Pepkowitz S, Prezant TR, Graham JM.
    Am J Med Genet; 1995 May 08; 56(4):359-65. PubMed ID: 7604844
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  • 14. Trisomy/partial monosomy 13 mosaicism associated with relatively mild clinical malformation.
    Duckett DP, Porter HJ, Young ID.
    Ann Genet; 1992 May 08; 35(2):113-6. PubMed ID: 1524408
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  • 15. Trisomy 9 mosaicism in a girl with multiple malformations.
    Diaz-Mares L, Molina B, Carnevale A.
    Ann Genet; 1990 May 08; 33(3):165-8. PubMed ID: 2288462
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  • 17. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
    Gentile M, Buonadonna AL, Cariola F, Fiorente P, Valenzano MC, Guanti G.
    J Med Genet; 1999 Jan 08; 36(1):77-82. PubMed ID: 9950374
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  • 18. 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 Jan 08; 51(4):303-14. PubMed ID: 18495567
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  • 19. Prenatal diagnosis and fetopathological findings in five fetuses with trisomy 9.
    Chitayat D, Hodgkinson K, Luke A, Winsor E, Rose T, Kalousek D.
    Am J Med Genet; 1995 Apr 10; 56(3):247-51. PubMed ID: 7778583
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  • 20. 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
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