BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 24036431)

  • 1. Prenatal diagnosis of de novo interstitial deletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect.
    Chen CP; Huang MC; Chen YY; Chern SR; Wu PS; Chen YT; Su JW; Wang W
    Gene; 2013 Dec; 531(2):496-501. PubMed ID: 24036431
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes.
    Chen CP; Huang JP; Chen YY; Chern SR; Wu PS; Su JW; Pan CW; Wang W
    Gene; 2013 Sep; 527(2):636-41. PubMed ID: 23850725
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1.
    Chen CP; Hsieh CH; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):847-851. PubMed ID: 29241933
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2→p14).
    Chen CP; Lee MJ; Chern SR; Wu PS; Su JW; Chen YT; Lee MS; Wang W
    Gene; 2013 Oct; 529(2):351-6. PubMed ID: 23948085
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization.
    Chen CP; Lin CJ; Chen YY; Wang LK; Chern SR; Wu PS; Su JW; Chen LF; Town DD; Pan CW; Wang W
    Gene; 2013 Dec; 532(1):80-6. PubMed ID: 24055486
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Pure partial monosomy 3p (3p25.3 → pter): prenatal diagnosis and array comparative genomic hybridization characterization.
    Chen CP; Su YN; Chen CY; Su JW; Chern SR; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):435-9. PubMed ID: 23040932
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
    Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1.
    Chen CP; Lin MH; Chen YY; Chern SR; Chen YN; Wu PS; Pan CW; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2015 Oct; 54(5):592-6. PubMed ID: 26522117
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review.
    Chen CP; Huang JP; Chen YY; Chern SR; Wu PS; Su JW; Chen YT; Chen WL; Wang W
    Gene; 2013 Sep; 527(1):405-9. PubMed ID: 23791650
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis.
    Chen CP; Su JW; Chern SR; Kuo YL; Wu PS; Lee MS; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2015 Feb; 54(1):58-61. PubMed ID: 25675921
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.
    Chen CP; Tsai CH; Chern SR; Wu PS; Su JW; Lee CC; Chen YT; Chen WL; Chen LF; Wang W
    Gene; 2013 Oct; 529(1):163-8. PubMed ID: 23933417
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1→q31.1).
    Chen CP; Chang SJ; Chern SR; Wu PS; Chen YT; Su JW; Chen WL; Wang W
    Gene; 2013 Jun; 521(2):311-5. PubMed ID: 23545313
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.
    Chen CP; Lin CJ; Chang TY; Chern SR; Wu PS; Chen YT; Su JW; Lee CC; Chen LF; Wang W
    Gene; 2013 Apr; 519(1):164-8. PubMed ID: 23403238
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review.
    Chen CP; Su YN; Chen CY; Chern SR; Wu PS; Su JW; Lee CC; Chen LF; Wang W
    Genomics; 2013 Oct; 102(4):265-9. PubMed ID: 23981964
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. First report of right sided interrupted aortic arch type A in combination with atrioventricular septal defect and microdeletion 22q11.
    Paech C; Kostelka M; Grothoff M
    Int J Cardiol; 2011 Nov; 152(3):397-8. PubMed ID: 21911270
    [No Abstract]   [Full Text] [Related]  

  • 19. Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review.
    Chen CP; Chang TY; Guo WY; Wu PC; Wang LK; Chern SR; Wu PS; Su JW; Chen YT; Chen LF; Wang W
    Gene; 2013 Dec; 532(1):152-9. PubMed ID: 24055730
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy.
    Chen CP; Lin SP; Liu YP; Chern SR; Wu PS; Su JW; Chen YT; Lee CC; Wang W
    Gene; 2013 Oct; 529(1):176-80. PubMed ID: 23933416
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.