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Journal Abstract Search

213 related items for PubMed ID: 9110370

  • 1. The use of interphase FISH for prenatal diagnosis of Pallister-Killian syndrome.
    Mowery-Rushton PA, Stadler MP, Kochmar SJ, McPherson E, Surti U, Hogge WA.
    Prenat Diagn; 1997 Mar; 17(3):255-65. PubMed ID: 9110370
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  • 3. Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome.
    Chen CP, Peng CR, Chern SR, Kuo YL, Wu PS, Town DD, Pan CW, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2014 Dec; 53(4):566-71. PubMed ID: 25510702
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  • 6. 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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  • 7. Pallister-Killian syndrome: normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growing epidermal cells, but mosaic tetrasomy 12p in skin fibroblasts.
    Horn D, Majewski F, Hildebrandt B, Körner H.
    J Med Genet; 1995 Jan 03; 32(1):68-71. PubMed ID: 7897632
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  • 8. Pallister-Killian syndrome [i(12p)]: first pre-natal diagnosis using cordocentesis in the second trimester confirmed by in situ hybridization.
    Chiesa J, Hoffet M, Rousseau O, Bourgeois JM, Sarda P, Mares P, Bureau JP.
    Clin Genet; 1998 Oct 03; 54(4):294-302. PubMed ID: 9831340
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  • 10. Pallister-Killian syndrome: difficulties of prenatal diagnosis.
    Doray B, Girard-Lemaire F, Gasser B, Baldauf JJ, De Geeter B, Spizzo M, Zeidan C, Flori E.
    Prenat Diagn; 2002 Jun 03; 22(6):470-7. PubMed ID: 12116305
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  • 11. Pallister-Killian syndrome: Multiband FISH of tetrasomy 12p.
    Gerdes AM, Hansen LK, Brandrup F, Soegaard K, Christoffersen A, Rasmussen K.
    Pediatr Dermatol; 2006 Jun 03; 23(4):378-81. PubMed ID: 16918638
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  • 12. aCGH detects partial tetrasomy of 12p in blood from Pallister-Killian syndrome cases without invasive skin biopsy.
    Theisen A, Rosenfeld JA, Farrell SA, Harris CJ, Wetzel HH, Torchia BA, Bejjani BA, Ballif BC, Shaffer LG.
    Am J Med Genet A; 2009 May 03; 149A(5):914-8. PubMed ID: 19353629
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  • 13. A case of mosaic tetrasomy 12p (Pallister-Killian Syndrome) diagnosed prenatally: comparison of chromosome analyses of various cells obtained from the patient.
    Takakuwa K, Hataya I, Arakawa M, Tamura M, Sekizuka N, Tanaka K.
    Am J Perinatol; 1997 Nov 03; 14(10):641-3. PubMed ID: 9605253
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  • 14. [Prenatally diagnosed case of Pallister‒Killian syndrome].
    Tidrenczel Z, P Tardy E, Sarkadi E, Simon J, Beke A, Demeter J.
    Orv Hetil; 2018 May 03; 159(21):847-852. PubMed ID: 29779390
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  • 15. 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 03; 53(3):361-4. PubMed ID: 15750020
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  • 17. New diagnostic method for Pallister-Killian syndrome: detection of i(12p) in interphase nuclei of buccal mucosa by fluorescence in situ hybridization.
    Ohashi H, Ishikiriyama S, Fukushima Y.
    Am J Med Genet; 1993 Jan 01; 45(1):123-8. PubMed ID: 8418650
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  • 18. Pallister-Killian syndrome: a study of 22 British patients.
    Blyth M, Maloney V, Beal S, Collinson M, Huang S, Crolla J, Temple IK, Baralle D.
    J Med Genet; 2015 Jul 01; 52(7):454-64. PubMed ID: 25888713
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  • 19. Pallister Killian--mosaic tetrasomy 12 p syndrome. Another prenatally diagnosed case.
    Bresson JL, Arbez-Gindre F, Peltie J, Gouget A.
    Prenat Diagn; 1991 Apr 01; 11(4):271-5. PubMed ID: 1896413
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  • 20. Pallister-Killian and Fryns syndromes: nosology.
    McPherson EW, Ketterer DM, Salsburey DJ.
    Am J Med Genet; 1993 Aug 15; 47(2):241-5. PubMed ID: 8213912
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