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 *

180 related articles for article (PubMed ID: 21671377)

  • 1. Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization.
    Li P; Pomianowski P; DiMaio MS; Florio JR; Rossi MR; Xiang B; Xu F; Yang H; Geng Q; Xie J; Mahoney MJ
    Am J Med Genet A; 2011 Jul; 155A(7):1605-15. PubMed ID: 21671377
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
    Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Comparative genomic hybridization: the profile of chromosomal imbalances in rhabdomyosarcoma].
    Li QX; Liu CX; Chun CP; Qi Y; Chang B; Nong WX; Yao ES; Li HA; Li F
    Zhonghua Bing Li Xue Za Zhi; 2008 Aug; 37(8):536-41. PubMed ID: 19094465
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosomal imbalances revealed in primary rhabdomyo-sarcomas by comparative genomic hybridization.
    Li QX; Liu CX; Chun CP; Qi Y; Chang B; Li XX; Chen YZ; Nong WX; Li HA; Li F
    Chin Med J (Engl); 2009 Jun; 122(11):1277-82. PubMed ID: 19567137
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Array comparative genomic hybridization in prenatal diagnosis: another experience.
    Vialard F; Molina Gomes D; Leroy B; Quarello E; Escalona A; Le Sciellour C; Serazin V; Roume J; Ville Y; de Mazancourt P; Selva J
    Fetal Diagn Ther; 2009; 25(2):277-84. PubMed ID: 19521095
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization.
    Chen CP; Chen YY; Chern SR; Wu PS; Su JW; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2013 Jun; 52(2):278-84. PubMed ID: 23915866
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular cytogenetic characterization of esophageal cancer detected by comparative genomic hybridization.
    Chang YC; Yeh KT; Liu TC; Chang JG
    J Clin Lab Anal; 2010; 24(3):167-74. PubMed ID: 20486198
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis and molecular cytogenetic characterization of three chromosomal abnormalities with favorable outcomes.
    Chen Q; Xu Z; Chen G; Liu S; Xia Y
    Taiwan J Obstet Gynecol; 2020 Mar; 59(2):338-341. PubMed ID: 32127162
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genomic aberrations in carcinomas of the uterine corpus.
    Micci F; Teixeira MR; Haugom L; Kristensen G; Abeler VM; Heim S
    Genes Chromosomes Cancer; 2004 Jul; 40(3):229-46. PubMed ID: 15139002
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Comprehensive molecular cytogenetic characterization of cervical cancer cell lines.
    Harris CP; Lu XY; Narayan G; Singh B; Murty VV; Rao PH
    Genes Chromosomes Cancer; 2003 Mar; 36(3):233-41. PubMed ID: 12557223
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cytogenetic aberrations in primary and recurrent fibrolamellar hepatocellular carcinoma detected by comparative genomic hybridization.
    Wilkens L; Bredt M; Flemming P; Kubicka S; Klempnauer J; Kreipe H
    Am J Clin Pathol; 2000 Dec; 114(6):867-74. PubMed ID: 11338475
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia.
    Chen CP; Wang YL; Chern SR; Liu YP; Peng CR; Kuo YL; Wu PS; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2015 Feb; 54(1):66-70. PubMed ID: 25675923
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: study of two cases and review of the literature.
    Rossi MR; DiMaio MS; Xiang B; Lu K; Kaymakcalan H; Seashore M; Mahoney MJ; Li P
    Am J Med Genet A; 2009 Dec; 149A(12):2788-94. PubMed ID: 19921640
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Detection of chromosomal DNA imbalance in medulloblastoma by comparative genomic hybridization].
    Sun YJ; Yu SZ; Sun CY; Wang Q; Jin SM; Wu WX; An TL
    Zhonghua Bing Li Xue Za Zhi; 2010 Sep; 39(9):606-10. PubMed ID: 21092588
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
    Yan Y; Wu Q; Zhang L; Wang X; Dan S; Deng D; Sun L; Yao L; Ma Y; Wang L
    Ultrasound Obstet Gynecol; 2014 Apr; 43(4):404-12. PubMed ID: 24323407
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Patterns of chromosomal aberrations in metastasizing and nonmetastasizing squamous cell carcinomas of the oropharynx and hypopharynx.
    Welkoborsky HJ; Bernauer HS; Riazimand HS; Jacob R; Mann WJ; Hinni ML
    Ann Otol Rhinol Laryngol; 2000 Apr; 109(4):401-10. PubMed ID: 10778896
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.