BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

974 related articles for article (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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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; 19(4):356-60. PubMed ID: 15192296
    [TBL] [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; 17(1):57-63. PubMed ID: 16719278
    [TBL] [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
    [TBL] [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; 18(2):217-26. PubMed ID: 17710874
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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; 516(1):138-42. PubMed ID: 23266815
    [TBL] [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; 19(10):986-9. PubMed ID: 10521829
    [TBL] [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; 25(2):112-8. PubMed ID: 15712324
    [TBL] [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; 50(2):205-11. PubMed ID: 21791309
    [TBL] [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; 23(6):504-8. PubMed ID: 12813767
    [TBL] [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; 49(4):473-80. PubMed ID: 21199750
    [TBL] [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; 55(2):288-92. PubMed ID: 27125417
    [TBL] [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; 25(6):451-5. PubMed ID: 15966060
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 49.