BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 23266815)

  • 1. 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]  

  • 2. 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]  

  • 3. Prenatal diagnosis of de novo partial trisomy 18p and partial monosomy 18q recurrent in a family with fatal aortic coarctation.
    Hu H; Hao J; Yao H; Chang Q; Li R; Zhang X; Liang Z
    Gene; 2013 Mar; 517(1):132-6. PubMed ID: 23232358
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 --> qter) and partial monosomy 6q(6q26 --> qter) by high-resolution array CGH.
    Choy KW; Chan LW; Tang MH; Ng LK; Leung TY; Lau TK
    J Matern Fetal Neonatal Med; 2009 Nov; 22(11):1014-20. PubMed ID: 19900039
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints.
    Chen CP; Chang YL; Chern SR; Wu PS; Su JW; Chen WL; Chen LF; Wang W
    Gene; 2013 Mar; 516(1):132-7. PubMed ID: 23266805
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Partial trisomy of the long arm of chromosome 1: prenatal diagnosis, clinical evaluation and cytogenetic findings. Case report and review of the literature.
    Cambosu F; Capobianco G; Fogu G; Bandiera P; Pirino A; Moro MA; Sanna R; Soro G; Dessole M; Montella A
    J Obstet Gynaecol Res; 2013 Feb; 39(2):592-7. PubMed ID: 22925348
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
    Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R
    Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31 →qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization.
    Chen CP; Su YN; Young RS; Tsai FJ; Wu PC; Chern SR; Town DD; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):506-12. PubMed ID: 21199755
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Trisomy 1q42-qter associated with monosomy 6q27-qter: a case report.
    Tartaglia E; Mastrantonio P; Costa D; Giugliano B; Porcellini A; Costagliola C
    Eur J Ophthalmol; 2011; 21(3):315-9. PubMed ID: 20954143
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results.
    Chen CP; Liou JD; Seow KM; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2020 Sep; 59(5):758-762. PubMed ID: 32917332
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Hsu CY; Wu PC; Town DD; Lee DJ; Ma GC; Wang W
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):320-6. PubMed ID: 21056318
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
    Chen CP; Su YN; Hsu CY; Chern SR; Lee CC; Chen YT; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):485-91. PubMed ID: 22212322
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.