BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

427 related articles for article (PubMed ID: 27343326)

  • 1. Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction.
    Chen CP; Ko TM; Huang WC; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Pan CW; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Jun; 55(3):415-8. PubMed ID: 27343326
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Lee MS; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):705-711. PubMed ID: 27751420
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
    Chen CP; Su YN; Chern SR; Hsu CY; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2011 Mar; 50(1):67-73. PubMed ID: 21482378
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound.
    Chen CP; Wang LK; Wu PC; Chang TY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Feb; 56(1):102-105. PubMed ID: 28254208
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization.
    Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):698-703. PubMed ID: 31542096
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
    Chen CP; Ko TM; Su YN; Wang LK; Chern SR; Wu PS; Chen YN; Chen SW; Ko K; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):733-737. PubMed ID: 27751426
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular cytogenetic characterization of del(X)(p22.33)mat and de novo dup(4)(q34.3q35.2) in a male fetus with multiple anomalies of facial dysmorphism, ventriculomegaly, congenital heart defects, short long bones and clinodactyly.
    Chen CP; Huang JP; Chen YY; Chen SW; Chern SR; Wu PS; Wu FT; Pan YT; Chen WL; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2023 May; 62(3):453-456. PubMed ID: 37188453
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
    Guo WJ; Callif-Daley F; Zapata MC; Miller ME
    Am J Med Genet; 1995 Sep; 58(3):230-6. PubMed ID: 8533823
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular characterization of inv dup del(8p): analysis of five cases.
    Shimokawa O; Kurosawa K; Ida T; Harada N; Kondoh T; Miyake N; Yoshiura K; Kishino T; Ohta T; Niikawa N; Matsumoto N
    Am J Med Genet A; 2004 Jul; 128A(2):133-7. PubMed ID: 15214003
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Structural abnormalities of chromosome 8 and fetoplacental discrepancy: A second case report and review of fetal phenotype of 8p inverted duplication deletion syndrome.
    Huynh MT; Riteau AS; Moradkhani K; Pichon O; Richard S; Joubert M; Bézieau S
    Eur J Med Genet; 2021 Jan; 64(1):104118. PubMed ID: 33248287
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
    Chen CP; Su YN; Chen YY; Su JW; Chern SR; Chen YT; Chen WL; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):506-11. PubMed ID: 22212326
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fetoplacental discrepancy involving structural abnormalities of chromosome 8 detected by prenatal diagnosis.
    Soler A; Sánchez A; Carrió A; Badenas C; Milà M; Borrell A
    Prenat Diagn; 2003 Apr; 23(4):319-22. PubMed ID: 12673638
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound.
    Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2020 Jul; 59(4):598-603. PubMed ID: 32653137
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Fluorescence in situ hybridization and single nucleotide polymorphism of a new case with inv dup del(8p).
    Caglayan AO; Engelen JJ; Ghesquiere S; Alofs M; Saatci C; Dundar M
    Genet Couns; 2009; 20(4):333-40. PubMed ID: 20162868
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
    Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY
    Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome.
    Chen CP; Lin SP; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):728-732. PubMed ID: 27751425
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dextrocardia, atrial septal defect, severe developmental delay, facial anomalies, and supernumerary ribs in a child with a complex unbalanced 8;22 translocation including partial 8p duplication.
    Pope K; Samanich J; Ramesh KH; Cannizzaro L; Pan Q; Babcock M
    Am J Med Genet A; 2012 Mar; 158A(3):641-7. PubMed ID: 22302699
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result.
    Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2021 Jul; 60(4):775-777. PubMed ID: 34247824
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.