BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 23705081)

  • 1. Prenatal Diagnosis of a Fetus with de novo Supernumerary Ring Chromosome 16 Characterized by Array Comparative Genomic Hybridization.
    Cignini P; Dinatale A; D'Emidio L; Giacobbe A; Pappalardo EM; Ermito S; Bizzoco D; Di Giacomo G; Gabrielli I; Mesoraca A; Giorlandino M; Giorlandino C
    AJP Rep; 2011 Sep; 1(1):29-32. PubMed ID: 23705081
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Prenatal diagnosis of a fetus with a ring chromosome 20 characterized by array-CGH.
    Cignini P; Dugo N; Giorlandino C; Gauci R; Spata A; Capriglione S; Cafà EV
    J Prenat Med; 2012 Oct; 6(4):72-3. PubMed ID: 23272278
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.
    Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chang SP; Yang CW; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):527-533. PubMed ID: 28805612
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
    Chen CP; Chen M; Ko TM; Ma GC; Tsai FJ; Tsai MS; Wu PC; Lee CC; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):500-5. PubMed ID: 21199754
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatally diagnosed de novo segmental amplification or deletion by microarray-based comparative genomic hybridization: A retrospective study.
    Peng HH; Lee CH; Su SY; Chen KJ; Lee YC; You SH; Lee WF; Cheng PJ
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):662-666. PubMed ID: 31542089
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis of ring chromosome 6 in a fetus with hydrocephalus.
    Walker ME; Lynch-Salamon DA; Milatovich A; Saal HM
    Prenat Diagn; 1996 Sep; 16(9):857-61. PubMed ID: 8905901
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3.
    Christopoulou G; Tzetis M; Konstantinidou AE; Tsezou A; Kanavakis E; Kitsiou-Tzeli S; Velissariou V
    Eur J Med Genet; 2012 Jan; 55(1):75-9. PubMed ID: 21914491
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report.
    Mohammadi R; Taheri R; Shahriyari F; Feiz F; Mohammadi Z; Shirian S; Raoofian R; Malekpour A; Pazhoomand R
    Int J Reprod Biomed; 2021 May; 19(5):477-482. PubMed ID: 34278202
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.
    Chen CP; Lin SP; Lin YH; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):852-855. PubMed ID: 28040132
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes.
    Chen CP; Lo LM; Ko TM; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Chen LF; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):331-334. PubMed ID: 33678337
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.
    Chen CP; Ko TM; Chern SR; Wu PS; Chen SW; Lai ST; Yang CW; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):545-549. PubMed ID: 28805616
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Prenatal diagnosis of a 1.651-Mb 19q13.42-q13.43 microdeletion in a fetus with micrognathia and bilateral pyelectasis on prenatal ultrasound.
    Chen CP; Hsu CY; Chern SR; Wu PS; Chen SW; Wu FT; Wang W
    Taiwan J Obstet Gynecol; 2020 Sep; 59(5):763-765. PubMed ID: 32917333
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization.
    Cain CC; Saul DO; Oehler E; Blakemore K; Stetten G
    Fetal Diagn Ther; 2008; 24(3):286-90. PubMed ID: 18818501
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Lee CC; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2020 Jan; 59(1):130-134. PubMed ID: 32039781
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
    Melo JB; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch JR; Kosyakova N; Ewers E; Liehr T; Carreira IM
    Cytogenet Genome Res; 2009; 125(2):109-14. PubMed ID: 19729913
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.