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972 related items for PubMed ID: 16506269

  • 1. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP, Chern SR, Lin CC, Wang TH, Li YC, Hsieh LJ, Lee CC, Hua HM, Wang W.
    Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP, Chern SR, Wang W, Lee CC, Chen WL, Chen LF, Chang TY, Tzen CY.
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP, Chern SR, Wang TH, Hsueh DW, Lee CC, Town DD, Wang W, Ko TM.
    Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
    [Abstract] [Full Text] [Related]

  • 4. Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
    Chen CP, Chern SR, Lee CC, Chen LF, Chin DT, Tzen CY, Wang W.
    Prenat Diagn; 2003 Sep; 23(9):758-61. PubMed ID: 12975789
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping.
    Hsieh LJ, Hsieh TC, Yeh GP, Lin MI, Chen M, Wang BB.
    Fetal Diagn Ther; 2004 Sep; 19(4):356-60. PubMed ID: 15192296
    [Abstract] [Full Text] [Related]

  • 6. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Huang JK, Lee CC, Wang W.
    Genet Couns; 2006 Sep; 17(1):57-63. PubMed ID: 16719278
    [Abstract] [Full Text] [Related]

  • 7. A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
    Chen CP, Huang HK, Ling PY, Su YN, Chen M, Tsai FJ, Wu PC, Chern SR, Chen YT, Lee CC, Wang W.
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):492-8. PubMed ID: 22212323
    [Abstract] [Full Text] [Related]

  • 8. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M, Hemly NA, Zaki MS.
    Genet Couns; 2007 Dec; 18(2):217-26. PubMed ID: 17710874
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis of partial trisomy 12q: clinical presentations and outcome.
    Peng HH, Wang TH, Hsueh DW, Chang SD, Soong YK.
    Prenat Diagn; 2005 Jun; 25(6):470-4. PubMed ID: 15966037
    [Abstract] [Full Text] [Related]

  • 10. Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes.
    Chen CP, Lin SP, Su YN, Tsai FJ, Wu PC, Town DD, Chen LF, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2012 Mar; 51(1):93-9. PubMed ID: 22482977
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->ter-->qter).
    Chen CP, Lin CC, Chang TY, Li YC, Hsieh LJ, Lee CC, Chen LF, Wang W.
    Prenat Diagn; 2006 Aug; 26(8):757-9. PubMed ID: 16865745
    [No Abstract] [Full Text] [Related]

  • 12. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S, Kasakyan S, L'Herminé AC, Mairovitz V, Gautier E, Aubry MC, Benkhalifa M, Tachdjian G.
    Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold.
    Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Chen LF, Wang W.
    Gene; 2013 Mar 01; 516(1):138-42. PubMed ID: 23266815
    [Abstract] [Full Text] [Related]

  • 14. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
    Chen CP, Devriendt K, Lee CC, Chen WL, Wang W, Wang TY.
    Prenat Diagn; 1999 Oct 01; 19(10):986-9. PubMed ID: 10521829
    [Abstract] [Full Text] [Related]

  • 15. Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
    Chen CP, Lin SP, Lin CC, Li YC, Chern SR, Chen WM, Lee CC, Hsieh LJ, Wang W.
    Prenat Diagn; 2005 Feb 01; 25(2):112-8. PubMed ID: 15712324
    [Abstract] [Full Text] [Related]

  • 16. Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.
    Chen CP, Su YN, Tsai FJ, Lin MH, Wu PC, Chern SR, Lee CC, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2011 Jun 01; 50(2):205-11. PubMed ID: 21791309
    [Abstract] [Full Text] [Related]

  • 17. Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
    Chen CP, Lin SP, Chern SR, Shih SL, Lee CC, Wang W, Liao YW.
    Prenat Diagn; 2003 Jun 01; 23(6):504-8. PubMed ID: 12813767
    [Abstract] [Full Text] [Related]

  • 18. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
    Chen CP, Chen M, Su YN, Hsu CY, Tsai FJ, Chern SR, Wu PC, Lee CC, Wang W.
    Taiwan J Obstet Gynecol; 2010 Dec 01; 49(4):473-80. PubMed ID: 21199750
    [Abstract] [Full Text] [Related]

  • 19. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter).
    Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Wang W.
    Taiwan J Obstet Gynecol; 2016 Apr 01; 55(2):288-92. PubMed ID: 27125417
    [Abstract] [Full Text] [Related]

  • 20. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP, Jouannic JM, Bessières B, Borie C, Martin-Luis I, Fallet-Bianco C, Portnoï MF.
    Prenat Diagn; 2005 Jun 01; 25(6):451-5. PubMed ID: 15966060
    [Abstract] [Full Text] [Related]

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