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438 related items for PubMed ID: 9599652

  • 1. Trisomy (12p) with telocentric and pseudoisodicentric chromosome formation in a fetus.
    Plaja A, Mediano C, Farran I, Vendrell T, Toran N, Gili T, Sanchez MA, Sarret E.
    Ann Genet; 1998; 41(1):52-5. PubMed ID: 9599652
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of mosaic tetrasomy 5p.
    Park JP, Barefoot KH, Ornvold K, Berg SZ, Dossu JR, Mohandas TK.
    Prenat Diagn; 2001 May; 21(5):351-3. PubMed ID: 11360274
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR, Huff RW, Ridgway LE, Stratton RF, Moore CM.
    Am J Med Genet; 1994 Mar 01; 50(1):21-7. PubMed ID: 8160748
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  • 4. [Edwards syndrome--most frequent indications for genetic amniocentesis. Analysis of the last 5 years].
    Chuchracki M, Janiak J, Ziółkowska K, Sedziak A, Opala T.
    Przegl Lek; 2012 Mar 01; 69(10):1007-10. PubMed ID: 23421080
    [Abstract] [Full Text] [Related]

  • 5. Relationship between anomalies of phenotype and karyotype in human embryogenesis.
    Kuliev AM.
    Sov Genet; 1974 Jul 15; 8(7):910-20. PubMed ID: 4424716
    [No Abstract] [Full Text] [Related]

  • 6. Non-mosaic trisomy 16 in a third-trimester fetus.
    Yancey MK, Hardin EL, Pacheco C, Kuslich CD, Donlon TA.
    Obstet Gynecol; 1996 May 15; 87(5 Pt 2):856-60. PubMed ID: 8677115
    [Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.
    Habecker-Green JG, Naeem R, Gold H, O'Grady JP, Kanaan C, Bayer-Zwirello L, Murray MS, Cohn GM.
    J Perinatol; 1998 May 15; 18(5):395-8. PubMed ID: 9766419
    [Abstract] [Full Text] [Related]

  • 8. [Echographic detection of chromosomal anomalies apropos of trisomy 13 and 18].
    Aubry JP, Aubry MC, Henrion R, Boué J, Labbe F.
    J Genet Hum; 1982 Oct 15; 30(3):233-53. PubMed ID: 7153769
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  • 10. Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p.
    De Pater JM, Van Tintelen JP, Stigter R, Brouwers HA, Scheres JM.
    Genet Couns; 2000 Oct 15; 11(3):241-7. PubMed ID: 11043432
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery.
    Chen CP, Liu FF, Jan SW, Lin SP, Lan CC.
    Prenat Diagn; 1996 Mar 15; 16(3):270-5. PubMed ID: 8710784
    [Abstract] [Full Text] [Related]

  • 12. 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
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  • 14. 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 15; 27(2):257-74. PubMed ID: 3605212
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  • 15. 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 15; 27(2):275-83. PubMed ID: 3605213
    [Abstract] [Full Text] [Related]

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  • 17. [Trisomy of the short arm of chromosome 9].
    Rogóyski A, Babel M, Holtorp-Tyszkiewiczowa J.
    Pediatr Pol; 1989 Apr 15; 64(4):248-52. PubMed ID: 2628892
    [No Abstract] [Full Text] [Related]

  • 18. [Trisomy 5p: a report of 2 cases].
    Alvarez-Coca J, García-Alix A, Delicado A, González M, Escribá R, López Pajares I, Morena V, Peralta A.
    An Esp Pediatr; 1985 Mar 31; 22(4):288-92. PubMed ID: 4003955
    [Abstract] [Full Text] [Related]

  • 19. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb 31; 26(2):138-46. PubMed ID: 16470734
    [Abstract] [Full Text] [Related]

  • 20. Trisomy 20 mosaicism and nonmosaic trisomy 20: a report of 2 cases.
    Joó JG, Beke A, Tóth-Pál E, Hargitai B, Szigeti Z, Papp C, Papp Z.
    J Reprod Med; 2006 Mar 31; 51(3):209-12. PubMed ID: 16674019
    [Abstract] [Full Text] [Related]

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