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Journal Abstract Search

424 related items for PubMed ID: 8460851

  • 1. [A case of neonatal Pallister-Killian syndrome (tetrasomy 12p)].
    González de Dios J, García-Alix Pérez A, Díaz de Bustamante A, Delicado Navarro A, Arés Segura S, Salas Hernández S, Quero Jiménez J.
    An Esp Pediatr; 1993 Mar; 38(3):277-9. PubMed ID: 8460851
    [No Abstract] [Full Text] [Related]

  • 2. Pericardial agenesis and focal aplasia cutis in tetrasomy 12p (Pallister-Killian syndrome).
    Zakowski MF, Wright Y, Ricci A.
    Am J Med Genet; 1992 Feb 01; 42(3):323-5. PubMed ID: 1536171
    [Abstract] [Full Text] [Related]

  • 3. [Pallister-Killian syndrome and 12p tetrasomy: increased LDH-B activity].
    Antich Femenias J, Briones Godino MP, Vilaseca Busca MA, Girós Blasco ML, Campos Castelló J, Jaume Roig B, Clusellas Casals N.
    An Esp Pediatr; 1991 Jun 01; 34(6):459-62. PubMed ID: 1929015
    [No Abstract] [Full Text] [Related]

  • 4. Mosaic tetrasomy 12p: four new cases, and confirmation of the chromosomal origin of the supernumerary chromosome in one of the original Pallister-Mosaic syndrome cases.
    Warburton D, Anyane-Yeboa K, Francke U.
    Am J Med Genet; 1987 Jun 01; 27(2):275-83. PubMed ID: 3605213
    [Abstract] [Full Text] [Related]

  • 5. Pallister-Killian syndrome: report of one case.
    Wu HC, Lin LH, Tsai LP, Huang CH, Hung KL, Liao HT.
    Acta Paediatr Taiwan; 2006 Jun 01; 47(3):139-41. PubMed ID: 17078467
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. [Tetrasomy 12p (Pallister-Killian syndrome): possible diagnosis before the age of a year].
    Chrzanowska K, Fryns JP.
    J Genet Hum; 1989 Sep 15; 37(3):259-61. PubMed ID: 2625629
    [Abstract] [Full Text] [Related]

  • 8. Chromosomal mosaicism in the Killian/Teschler-Nicola syndrome.
    Raffel LJ, Mohandas T, Rimoin DL.
    Am J Med Genet; 1986 Aug 15; 24(4):607-11. PubMed ID: 3740095
    [Abstract] [Full Text] [Related]

  • 9. 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 15; 39(2):259-67. PubMed ID: 8086644
    [Abstract] [Full Text] [Related]

  • 10. Lethal presentation of mosaic tetrasomy 12p (Pallister-Killian) syndrome.
    Young ID, Duckett DP, O'Reilly KM.
    Ann Genet; 1989 Jun 15; 32(1):62-4. PubMed ID: 2751252
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 14(10):641-3. PubMed ID: 9605253
    [Abstract] [Full Text] [Related]

  • 12. Pallister-Killian and Fryns syndromes.
    Stratton RF, Moore CM, Popham CS, DuPont BR, Mattern VL.
    Am J Med Genet; 1994 May 15; 51(1):90. PubMed ID: 8030681
    [No Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of Pallister-Killian syndrome.
    Soukup S, Neidich K.
    Am J Med Genet; 1990 Apr 15; 35(4):526-8. PubMed ID: 1692181
    [Abstract] [Full Text] [Related]

  • 14. [Killian-Teschler-Nicola syndrome (Pallister-Killian syndrome, mosaic tetrasomy 12p)].
    Pankau R, Diebold U, Jenderny J, Kautza M, Dörner K.
    Monatsschr Kinderheilkd; 1992 Jun 15; 140(6):340-2. PubMed ID: 1640944
    [No Abstract] [Full Text] [Related]

  • 15. Pallister-Killian syndrome: characterization of the isochromosome 12p by fluorescent in situ hybridization.
    Speleman F, Leroy JG, Van Roy N, De Paepe A, Suijkerbuijk R, Brunner H, Looijenga L, Verschraegen-Spae MR, Orye E.
    Am J Med Genet; 1991 Dec 01; 41(3):381-7. PubMed ID: 1789295
    [Abstract] [Full Text] [Related]

  • 16. Isochromosome 12p mosaicism (Pallister-Killian syndrome): newborn diagnosis by direct bone marrow analysis.
    Ward BE, Hayden MW, Robinson A.
    Am J Med Genet; 1988 Dec 01; 31(4):835-9. PubMed ID: 3239575
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 32(1):68-71. PubMed ID: 7897632
    [Abstract] [Full Text] [Related]

  • 18. Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases.
    Reynolds JF, Daniel A, Kelly TE, Gollin SM, Stephan MJ, Carey J, Adkins WN, Webb MJ, Char F, Jimenez JF.
    Am J Med Genet; 1987 Jun 01; 27(2):257-74. PubMed ID: 3605212
    [Abstract] [Full Text] [Related]

  • 19. The Pallister-Killian syndrome in an African individual.
    Woodman BF, Jordan MA, Moller LI, Cartwright JD, De Ravel TJ.
    Genet Couns; 1995 Jun 01; 6(1):33-6. PubMed ID: 7794559
    [Abstract] [Full Text] [Related]

  • 20. Tissue-limited mosaicism in Pallister-Killian syndrome -- a case in point.
    Choo S, Teo SH, Tan M, Yong MH, Ho LY.
    J Perinatol; 2002 Jun 01; 22(5):420-3. PubMed ID: 12082482
    [Abstract] [Full Text] [Related]

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