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144 related items for PubMed ID: 1287646

  • 1. Prenatal diagnosis of Pallister-Killian syndrome: resolution of cytogenetic ambiguity by use of fluorescent in situ hybridization.
    McLean S, Stanley W, Stern H, Fonda-Allen J, Devine G, Ellingham T, Rosenbaum K.
    Prenat Diagn; 1992 Dec; 12(12):985-91. PubMed ID: 1287646
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  • 2. 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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  • 3. Pallister-Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis.
    Libotte F, Bizzoco D, Gabrielli I, Mesoraca A, Cignini P, Vitale SG, Marilli I, Gulino FA, Rapisarda AM, Giorlandino C.
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):863-866. PubMed ID: 28040135
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  • 9. [Prenatally diagnosed case of Pallister‒Killian syndrome].
    Tidrenczel Z, P Tardy E, Sarkadi E, Simon J, Beke A, Demeter J.
    Orv Hetil; 2018 May; 159(21):847-852. PubMed ID: 29779390
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  • 10. 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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  • 12. Mosaic tetrasomy 12p.
    Gilgenkrantz S, Droulle P, Schweitzer M, Foliguet B, Chadefaux B, Lombard M, Chery M, Prieur M.
    Clin Genet; 1985 Dec; 28(6):495-502. PubMed ID: 2934184
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  • 13. Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker.
    Dufke A, Walczak C, Liehr T, Starke H, Trifonov V, Rubtsov N, Schöning M, Enders H, Eggermann T.
    Eur J Hum Genet; 2001 Aug; 9(8):572-6. PubMed ID: 11528501
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  • 16. Tissue-limited mosaicism in Pallister-Killian syndrome -- a case in point.
    Choo S, Teo SH, Tan M, Yong MH, Ho LY.
    J Perinatol; 2002 Aug; 22(5):420-3. PubMed ID: 12082482
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  • 17. 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; 14(10):641-3. PubMed ID: 9605253
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  • 18. 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; 53(3):361-4. PubMed ID: 15750020
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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; 11(4):271-5. PubMed ID: 1896413
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  • 20. Prenatal diagnosis of Pallister-Killian syndrome associated with pulmonary stenosis and right ventricular dilatation.
    Park IY, Shin JC, Kwon JY, Koo BK, Kim M, Lim J, Kim Y, Han K.
    Korean J Lab Med; 2009 Aug; 29(4):366-70. PubMed ID: 19726901
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