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Journal Abstract Search

182 related items for PubMed ID: 9489799

  • 1. New case of mosaic tetrasomy 9p with additional neurometabolic findings.
    Eggermann T, Rossier E, Theurer-Mainka U, Backsch C, Klein-Vogler U, Enders H, Kaiser P.
    Am J Med Genet; 1998 Feb 17; 75(5):530-3. PubMed ID: 9489799
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  • 2. Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature.
    Eggermann T, Schubert R, Engels H, Apacik C, Stengel-Rutkowski S, Haefliger C, Emiliani V, Ricagni C, Schwanitz G.
    Ann Genet; 1999 Feb 17; 42(2):75-80. PubMed ID: 10434120
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  • 5. New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girl.
    de Azevedo Moreira LM, Freitas LM, Gusmão FA, Riegel M.
    Birth Defects Res A Clin Mol Teratol; 2003 Dec 17; 67(12):985-8. PubMed ID: 14745919
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  • 6. Tetrasomy 9p mosaicism associated with a normal phenotype in two cases.
    Papoulidis I, Kontodiou M, Tzimina M, Saitis I, Hamid AB, Klein E, Kosyakova N, Kordass U, Kunz J, Siomou E, Nicolaides P, Orru S, Thomaidis L, Liehr T, Petersen MB, Manolakos E.
    Cytogenet Genome Res; 2012 Dec 17; 136(4):237-41. PubMed ID: 22487875
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  • 7. Isochromosomes 12p and 9p: parental origin and possible mechanisms of formation.
    Dutly F, Balmer D, Baumer A, Binkert F, Schinzel A.
    Eur J Hum Genet; 1998 Dec 17; 6(2):140-4. PubMed ID: 9781058
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  • 9. Tissue limited mosaicism in a patient with tetrasomy 9p.
    Papenhausen P, Riscile G, Miller K, Kousseff B, Tedesco T.
    Am J Med Genet; 1990 Nov 17; 37(3):388-91. PubMed ID: 2260570
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  • 10. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A, Kitsiou S, Fryssira H, Sofocleous C, Kouvidi E, Tsangaris GT, Salavoura K, Mavrou A.
    In Vivo; 2006 Nov 17; 20(4):473-8. PubMed ID: 16900777
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  • 12. Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding?
    Reish O, Wolach B, Amiel A, Kedar I, Dolfin T, Fejgin M.
    Am J Med Genet; 1998 Apr 28; 77(1):72-5. PubMed ID: 9557898
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  • 14. Mosaic tetrasomy 8p: molecular cytogenetic confirmation and measurement of glutathione reductase and tissue plasminogen activator levels.
    Fisher AM, Barber JC, Crolla JA, James RS, Lestas AN, Jennings I, Dennis NR.
    Am J Med Genet; 1993 Aug 01; 47(1):100-5. PubMed ID: 8368238
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  • 15. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J, Kimijima Y, Yamada S, Amagasa T, Saito-Ohara F.
    J Craniomaxillofac Surg; 2000 Jun 01; 28(3):165-70. PubMed ID: 10964553
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  • 16. Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)].
    Sijmons RH, Leegte B, van Lingen RA, de Pater JM, van der Veen AY, del Canho H, Bos C, ten Kate LP, Breed AS.
    Am J Med Genet; 1993 Sep 15; 47(4):559-62. PubMed ID: 7504882
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  • 17. Tetrasomy 12p--unusual presentation in CVS.
    Dong L, Falk RE, Williams J, Kohan M, Schreck RR.
    Prenat Diagn; 2003 Feb 15; 23(2):101-3. PubMed ID: 12575013
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  • 18. Report of two new cases of Pallister-Killian syndrome confirmed by FISH: tissue-specific mosaicism and loss of i(12p) by in vitro selection.
    Schubert R, Viersbach R, Eggermann T, Hansmann M, Schwanitz G.
    Am J Med Genet; 1997 Oct 03; 72(1):106-10. PubMed ID: 9295085
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  • 19. Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH).
    Petty EM, Gibson LH, Breg WR, Burns JP, Yang-Feng TL.
    Am J Med Genet; 1993 Mar 15; 45(6):770-3. PubMed ID: 8456860
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  • 20. Pallister-Killian syndrome: rapid decrease of isochromosome 12p frequency during amniocyte subculturing. Conclusion for strategy of prenatal cytogenetic diagnostics.
    Polityko AD, Goncharova E, Shamgina L, Drozdovskaja N, Podleschuk L, Abramchik E, Jaroshevich E, Khurs O, Pisarik I, Pribushenya O, Rumyantseva N, Naumchik I.
    J Histochem Cytochem; 2005 Mar 15; 53(3):361-4. PubMed ID: 15750020
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