These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 23040946)

  • 1. Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester.
    Chen CP; Su YN; Weng SL; Tsai FJ; Chen CY; Liu YP; Chern SR; Chen WL; Wu PC; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):481-4. PubMed ID: 23040946
    [No Abstract]   [Full Text] [Related]  

  • 2. Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
    Chen CP; Su YN; Su JW; Chern SR; Chen YT; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2013 Mar; 52(1):97-105. PubMed ID: 23548227
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism.
    Chen CP; Chen YY; Chern SR; Wu PS; Su JW; Chen YT; Lee CC; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2013 Sep; 52(3):395-400. PubMed ID: 24075380
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism.
    Chen CP; Huang HK; Su YN; Chern SR; Su JW; Lee CC; Town DD; Chen WL; Chen YT; Wang W
    Taiwan J Obstet Gynecol; 2012 Mar; 51(1):77-82. PubMed ID: 22482973
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly.
    Chen CP; Su YN; Chen YY; Chern SR; Su JW; Chen YT; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):471-4. PubMed ID: 23040944
    [No Abstract]   [Full Text] [Related]  

  • 6. Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review.
    Chen CP; Chern SR; Chen YN; Wu PS; Yang CW; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2015 Aug; 54(4):426-31. PubMed ID: 26384064
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis.
    Chen CP; Chang SD; Su YN; Chen M; Chern SR; Su JW; Chen YT; Chen WL; Pan CW; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):405-10. PubMed ID: 23040926
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
    Chen CP; Lin HM; Su YN; Chern SR; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):341-50. PubMed ID: 21056321
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Rapid genome-wide aneuploidy diagnosis using uncultured amniocytes and array comparative genomic hybridization in pregnancy with abnormal ultrasound findings detected in late second and third trimesters.
    Chen CP; Su YN; Tsai FJ; Chern SR; Hsu CY; Huang MC; Wang W
    Taiwan J Obstet Gynecol; 2010 Mar; 49(1):120-3. PubMed ID: 20466310
    [No Abstract]   [Full Text] [Related]  

  • 11. Terminal 2q deletion and distal 15q duplication: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes.
    Chen CP; Su YN; Tsai FJ; Lin HH; Chern SR; Lee MS; Hwang JK; Chen TH; Wang W
    Taiwan J Obstet Gynecol; 2009 Dec; 48(4):441-5. PubMed ID: 20045775
    [No Abstract]   [Full Text] [Related]  

  • 12. Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomalies.
    Karcaaltincaba D; Ceylaner S; Ceylaner G; Dalkilic S; Karli-Oguz K; Kandemir O
    Genet Couns; 2010; 21(1):19-24. PubMed ID: 20420025
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations.
    Chen CP; Su YN; Lin SY; Chang CL; Wang YL; Huang JP; Chen CY; Hung FY; Chen YY; Wu PC; Wang W
    Taiwan J Obstet Gynecol; 2011 Mar; 50(1):85-94. PubMed ID: 21482381
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia.
    Chen CP; Wang YL; Chern SR; Liu YP; Peng CR; Kuo YL; Wu PS; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2015 Feb; 54(1):66-70. PubMed ID: 25675923
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of trisomy 6 mosaicism.
    Destree A; Fourneau C; Dugauquier C; Rombout S; Sartenaer D; Gillerot Y
    Prenat Diagn; 2005 May; 25(5):354-7. PubMed ID: 15906424
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review.
    Chen CP; Chen M; Pan YJ; Su YN; Chern SR; Tsai FJ; Chen YT; Wang W
    Taiwan J Obstet Gynecol; 2011 Sep; 50(3):331-8. PubMed ID: 22030049
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatally diagnosed trisomy 20 mosaicism associated with arachnoid cyst of basal cistern.
    Stein QP; Boyle JG; Crotwell PL; Flanagan JD; Johnson KJ; Davis-Keppen L; Van Eerden P; Woltanski AR; Watson WJ
    Prenat Diagn; 2008 Dec; 28(12):1169-70. PubMed ID: 19003786
    [No Abstract]   [Full Text] [Related]  

  • 18. Is second-trimester genetic amniocentesis for trisomy 18 ever indicated in the presence of a normal genetic sonogram?
    Oyelese Y; Vintzileos AM
    Ultrasound Obstet Gynecol; 2005 Dec; 26(7):691-4. PubMed ID: 16308891
    [No Abstract]   [Full Text] [Related]  

  • 19. Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.
    Chen CP; Su YN; Chen YY; Chern SR; Liu YP; Wu PC; Lee CC; Chen YT; Wang W
    Taiwan J Obstet Gynecol; 2011 Sep; 50(3):345-52. PubMed ID: 22030051
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Application of fluorescence in situ hybridization to prenatal diagnosis of aneuploidy in 110 uncultured amniotic fluid samples].
    Liu H; Liao C; Huang YN; Pan M; Yi CX; Yuan SM; Hu SY; Zhong HZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):453-6. PubMed ID: 20677157
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.