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Journal Abstract Search

144 related items for PubMed ID: 1287646

  • 21.
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  • 22. 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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  • 23. The Pallister-Killian syndrome in a child with rare karyotype--a diagnostic problem.
    Smigiel R, Pilch J, Makowska I, Busza H, Slezak R, Sasiadek MM.
    Eur J Pediatr; 2008 Sep 03; 167(9):1063-5. PubMed ID: 18000682
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  • 24. 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 03; 52(7):454-64. PubMed ID: 25888713
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  • 25. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP, Ko TM, Chen YY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2017 Dec 03; 56(6):836-839. PubMed ID: 29241930
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  • 26.
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  • 28. Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization, and literature review.
    Chen CP, Wang LK, Chern SR, Wu PS, Chen YT, Kuo YL, Chen WL, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2014 Mar 03; 53(1):79-85. PubMed ID: 24767652
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  • 29. Cytogenetic study of a severe case of Pallister-Killian syndrome using fluorescence in situ hybridization.
    Gamal SM, Hasegawa T, Satoh H, Watanabe T, Endo K, Satoh Y.
    Jpn J Hum Genet; 1994 Jun 03; 39(2):259-67. PubMed ID: 8086644
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  • 30. Pallister-Killian syndrome: Review of fetal phenotype.
    Thakur S, Gupta R, Tiwari B, Singh N, Saxena KK.
    Clin Genet; 2019 Jan 03; 95(1):79-84. PubMed ID: 29790157
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  • 31.
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  • 32. Prenatal diagnosis of Pallister-Killian syndrome in pregnancy with normal CVS result and abnormal ultrasound findings in the second trimester.
    Frisova V, Svobodova IT, Tozzi M, Raskova D.
    Taiwan J Obstet Gynecol; 2018 Oct 03; 57(5):726-729. PubMed ID: 30342660
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  • 33.
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  • 34. 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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  • 35. Prenatal diagnosis of the Pallister-Killian mosaic aneuploidy syndrome by CVS.
    Bernert J, Bartels I, Gatz G, Hansmann I, Heyat M, Niedmann PD, Rehder H, Waldenmaier C, Zoll B.
    Am J Med Genet; 1992 Mar 01; 42(5):747-50. PubMed ID: 1632452
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  • 36. Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques.
    de Pater JM, Govaerts LC, de Man SA, van der Sijs-Bos CJ, Christiaens GC, van Dam WM, Loneus WH, Engelen JJ.
    Prenat Diagn; 2003 Sep 01; 23(9):747-51. PubMed ID: 12975787
    [Abstract] [Full Text] [Related]

  • 37. Prenatal diagnosis of mosaic tetrasomy 18p.
    Chen CP, Ko TM, Su YN, Chern SR, Su JW, Chen YT, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2012 Dec 01; 51(4):625-9. PubMed ID: 23276569
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  • 38. [Combined chromosomal microarray analysis and fluorescence in situ hybridization for prenatal diagnosis of two cases with Pallister-Killian syndrome].
    Wang T, Ren C, Guo L, Lu J, Chen H, Huang H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Jun 10; 36(6):571-573. PubMed ID: 31055807
    [Abstract] [Full Text] [Related]

  • 39. Using Array-Based Comparative Genomic Hybridization to Diagnose Pallister-Killian Syndrome.
    Lee MN, Lee J, Yu HJ, Lee J, Kim SH.
    Ann Lab Med; 2017 Jan 10; 37(1):66-70. PubMed ID: 27834069
    [Abstract] [Full Text] [Related]

  • 40. Tetrasomy 12p (Pallister-Killian syndrome): difficulties in prenatal diagnosis.
    Kunz J, Schoner K, Stein W, Rehder H, Fritz B.
    Arch Gynecol Obstet; 2009 Dec 10; 280(6):1049-53. PubMed ID: 19340439
    [Abstract] [Full Text] [Related]

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