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Journal Abstract Search

150 related items for PubMed ID: 9664211

  • 21. Mosaic trisomy r(14) associated with epilepsy and mental retardation.
    Tzoufi M, Kanioglou C, Dasoula A, Asproudis I, Tsatsoulis A, Sismani C, Patsalis PC, Georgiou I, Syrrou M.
    J Child Neurol; 2007 Jul; 22(7):869-73. PubMed ID: 17715281
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  • 22. 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 Jul; 59(6):444-8. PubMed ID: 18402336
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  • 24. Maternal uniparental disomy 14 dissection of the phenotype with respect to rare autosomal recessively inherited traits, trisomy mosaicism, and genomic imprinting.
    Kotzot D.
    Ann Genet; 2004 Jul; 47(3):251-60. PubMed ID: 15337470
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  • 27. Fluorescent in situ hybridization assessment of chromosome copy number in gestational trophoblastic disease.
    Mark HF, Grollino MG, Sulaiman RA, Lathrop JC.
    Ann Clin Lab Sci; 1995 Jul; 25(4):291-6. PubMed ID: 7668813
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  • 28. Pallister-Killian Syndrome (PKS) as a Cause of Mental Retardation.
    Shamdeen A, Meyer S, Gottschling S, Oehl-Jaschkowitz B, Gortner L, Shamdeen MG.
    Klin Padiatr; 2009 Jul; 221(2):97-9. PubMed ID: 19067289
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  • 31. Prenatal diagnosis of trisomy 6 mosaicism.
    Destree A, Fourneau C, Dugauquier C, Rombout S, Sartenaer D, Gillerot Y.
    Prenat Diagn; 2005 May; 25(5):354-7. PubMed ID: 15906424
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  • 33. Mosaic supernumerary r(8) syndrome.
    Yilmaz S, Tarkan-Argüden Y, Kuru D, Deviren A, Karaman B, Yüksel A, Hacihanefioğlu S.
    Genet Couns; 2005 May; 16(2):187-90. PubMed ID: 16080301
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  • 35. 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; 51(4):303-14. PubMed ID: 18495567
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  • 37. Disappearing trisomy 8 mosaicism.
    Mark HF, Bier JA.
    Ann Clin Lab Sci; 1997 May; 27(4):293-8. PubMed ID: 9210975
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  • 38. Histopathology and molecular cytogenetics of a corneal opacity associated with the trisomy 8 mosaic syndrome (46,XY/47,XY, +8).
    Scott JA, Howard PJ, Smith PA, Fryer A, Easty DL, Patterson A, Kaye SB.
    Cornea; 1997 Jan; 16(1):35-41. PubMed ID: 8985632
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  • 39. A case of trisomy 12 mosaicism with pituitary malformation and polycystic ovary syndrome.
    Boulard S, Diene G, Barat R, Oliver I, Pienkowski C, Lacombe D, Vincent MC, Bourrouillou G, Tauber M.
    Genet Couns; 2006 Jan; 17(2):173-83. PubMed ID: 16970035
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  • 40. Trisomy 14 Mosaicism: a case without evidence of neurodevelopmental delay and a review of the literature.
    Merritt TA, Natarajan G.
    Am J Perinatol; 2007 Oct; 24(9):563-6. PubMed ID: 17893842
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