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: 33466173)

  • 1. Prenatal diagnosis and ultrasonographic findings of partial trisomy of chromosome 6q: A case report and review of the literature.
    Li L; Yu Y; Zhang H; Jiang Y; Liu R; Zhang H
    Medicine (Baltimore); 2021 Jan; 100(2):e24091. PubMed ID: 33466173
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ultrasonographic findings and prenatal diagnosis of Jacobsen syndrome: A case report and review of the literature.
    Chen S; Wang R; Zhang X; Li L; Jiang Y; Liu R; Zhang H
    Medicine (Baltimore); 2020 Jan; 99(1):e18695. PubMed ID: 31895838
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis of Cri-du-Chat syndrome with concomitant distal trisomy 10q syndrome in one fetus with ultrasound anomalies.
    He JP; Qian Y; Liu WJ; Tang J; Qin MH; Luo SJ; Hou JH; Lv MX
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):318-323. PubMed ID: 33678334
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ultrasonographic findings and prenatal diagnosis of complete trisomy 17p syndrome: A case report and review of the literature.
    Li L; Zhang X; Shi Q; Li L; Jiang Y; Liu R; Zhang H
    J Clin Lab Anal; 2021 Jan; 35(1):e23582. PubMed ID: 32951212
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical, cytogenetic, and molecular findings in a fetus with ultrasonic multiple malformations, 4q duplication, and 7q deletion: A case report and literature review.
    Yue F; Jiang Y; Yu Y; Yang X; Zhang H; Liu R; Wang R
    Medicine (Baltimore); 2018 Nov; 97(45):e13094. PubMed ID: 30407316
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Partial trisomy 16q and partial monosomy 7p of a fetus derivated from paternal balanced translocation: A case report.
    Xie HH; Liu T; Zhang JB; Zhai JF; Liu Y
    Medicine (Baltimore); 2021 Feb; 100(7):e24382. PubMed ID: 33607772
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review.
    Chen CP; Huang MC; Chern SR; Wu PS; Chen SW; Chuang TY; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):692-697. PubMed ID: 31542095
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter).
    Chen CP; Hung FY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2016 Apr; 55(2):288-92. PubMed ID: 27125417
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Prenatal diagnosis of de novo isochromosome 4p with an unbalanced t(4;9) translocation in a fetus with congenital anomalies: A case report and literature review.
    Yao YY; Zhang CC; Bi H; Zhu F
    Taiwan J Obstet Gynecol; 2022 Jan; 61(1):157-162. PubMed ID: 35181031
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. A rare case of partial trisomy 8q24.12-q24.3 and partial monosomy of 8q24.3: Prenatal diagnosis and clinical findings.
    Farcas S; Erdelean D; Anne-Elise Szekely F; Navolan D; Andreescu N; Cioca A
    Taiwan J Obstet Gynecol; 2019 Jan; 58(1):36-39. PubMed ID: 30638476
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome.
    Chen CP; Chan CH; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2021 Jan; 60(1):152-156. PubMed ID: 33494992
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.