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Journal Abstract Search

194 related items for PubMed ID: 1287645

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  • 2. 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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  • 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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  • 5. Tissue-specific mosaicism among fetuses with prenatally diagnosed diaphragmatic hernia.
    Donnenfeld AE, Campbell TJ, Byers J, Librizzi RJ, Weiner S.
    Am J Obstet Gynecol; 1993 Oct; 169(4):1017-21. PubMed ID: 8238112
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  • 8. 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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  • 9. A further prenatal diagnosis of mosaic tetrasomy 12p (Pallister-Killian syndrome).
    Tejada MI, Uribarren A, Briones P, Vilaseca MA.
    Prenat Diagn; 1992 Jun; 12(6):529-34. PubMed ID: 1513756
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  • 10. 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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  • 11. 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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  • 12. 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; 32(1):68-71. PubMed ID: 7897632
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  • 15. Amniocentesis can be useful during the third trimester of pregnancy for antenatal diagnosis of Pallister-Killian syndrome: a case report.
    Murakami M, Iwasa T, Takahashi Y, Morine M.
    Clin Exp Obstet Gynecol; 2011 Jan; 38(3):269-71. PubMed ID: 21995162
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  • 16. Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.
    Micale MA, Wolff DJ, Dickerman LH, Redline R, Conroy JM, Schwartz S.
    Prenat Diagn; 1996 Oct; 16(10):893-7. PubMed ID: 8938057
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  • 19. Pallister-Killian syndrome: Review of fetal phenotype.
    Thakur S, Gupta R, Tiwari B, Singh N, Saxena KK.
    Clin Genet; 2019 Jan; 95(1):79-84. PubMed ID: 29790157
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