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 *

267 related articles for article (PubMed ID: 23703053)

  • 1. Trisomy 18: review of the clinical, etiologic, prognostic, and ethical aspects.
    Rosa RF; Rosa RC; Zen PR; Graziadio C; Paskulin GA
    Rev Paul Pediatr; 2013; 31(1):111-20. PubMed ID: 23703053
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Edwards syndrome--most frequent indications for genetic amniocentesis. Analysis of the last 5 years].
    Chuchracki M; Janiak J; Ziółkowska K; Sedziak A; Opala T
    Przegl Lek; 2012; 69(10):1007-10. PubMed ID: 23421080
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Phenotypic extremes in liveborn monozygotic twins with mosaic Edwards syndrome.
    Bussmann N; Cunningham K; Green A; Ryan CA
    BMJ Case Rep; 2015 Nov; 2015():. PubMed ID: 26561224
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Prenatal diagnosis of trisomy 13 and trisomy 18: the experience of Assaf-Harofe Medical Center].
    Naor Dovev M; Maymon R; Keidar R; Reish O; Melcer Y; Vaknin Z
    Harefuah; 2014 Aug; 153(8):453-7, 499, 498. PubMed ID: 25286634
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Using Patient-Centered Care After a Prenatal Diagnosis of Trisomy 18 or Trisomy 13: A Review.
    Haug S; Goldstein M; Cummins D; Fayard E; Merritt TA
    JAMA Pediatr; 2017 Apr; 171(4):382-387. PubMed ID: 28192554
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromosomal abnormalities: trisomy 18, trisomy 13, deletions, and microdeletions.
    Matthews AL
    J Perinat Neonatal Nurs; 1999 Sep; 13(2):59-75; quiz 103-4. PubMed ID: 10818854
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Antenatal detection of Edwards (Trisomy 18) and Patau (Trisomy 13) syndrome: England and Wales 2005-2012.
    Springett AL; Morris JK
    J Med Screen; 2014 Sep; 21(3):113-9. PubMed ID: 24993362
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center.
    Lau TK; Cheung SW; Lo PS; Pursley AN; Chan MK; Jiang F; Zhang H; Wang W; Jong LF; Yuen OK; Chan HY; Chan WS; Choy KW
    Ultrasound Obstet Gynecol; 2014 Mar; 43(3):254-64. PubMed ID: 24339153
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Trisomy 18: experience of a reference hospital from the south of Brazil.
    Rosa RF; Rosa RC; Lorenzen MB; de Moraes FN; Graziadio C; Zen PR; Paskulin GA
    Am J Med Genet A; 2011 Jul; 155A(7):1529-35. PubMed ID: 21671399
    [TBL] [Abstract][Full Text] [Related]  

  • 10. When Cri du chat syndrome meets Edwards syndrome.
    Xie Y; Zhou Y; Wu J; Sun Y; Chen Y; Chen B
    Mol Med Rep; 2015 Mar; 11(3):1933-8. PubMed ID: 25385231
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Systematic review of noninvasive prenatal diagnosis for abnormal chromosome genetic diseases using free fetal DNA in maternal plasma.
    Yang H; Xu HB; Liu TT; He XL
    Genet Mol Res; 2015 Sep; 14(3):10603-8. PubMed ID: 26400291
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Trisomy 18-Edwards syndrome: a report of three patients.
    Ejiwumni AB; Msamati BC
    Cent Afr J Med; 1993 May; 39(5):105-9. PubMed ID: 8131193
    [No Abstract]   [Full Text] [Related]  

  • 13. [Double aneuploidy (trisomy X, trisomy 18) in a newborn with trisomy 18 phenotype].
    Pachajoa H
    Arch Argent Pediatr; 2013; 111(4):e101-4. PubMed ID: 23912296
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Avoidance of emergency surgery in newborn infants with trisomy 18.
    Bos AP; Broers CJ; Hazebroek FW; van Hemel JO; Tibboel D; Wesby-van Swaay E; Molenaar JC
    Lancet; 1992 Apr; 339(8798):913-5. PubMed ID: 1348308
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An infant with trisomy 18 and a ventricular septal defect.
    Janvier A; Okah F; Farlow B; Lantos JD
    Pediatrics; 2011 Apr; 127(4):754-9. PubMed ID: 21402635
    [TBL] [Abstract][Full Text] [Related]  

  • 16. First-trimester screening for trisomies 18 and 13, triploidy and Turner syndrome by detailed early anomaly scan.
    Wagner P; Sonek J; Hoopmann M; Abele H; Kagan KO
    Ultrasound Obstet Gynecol; 2016 Oct; 48(4):446-451. PubMed ID: 26611869
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Birth prevalence and survival of exomphalos in england and wales: 2005 to 2011.
    Springett A; Draper ES; Rankin J; Rounding C; Tucker D; Stoianova S; Wellesley D; Morris JK
    Birth Defects Res A Clin Mol Teratol; 2014 Sep; 100(9):721-5. PubMed ID: 25178262
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A tumor profile in Edwards syndrome (trisomy 18).
    Satgé D; Nishi M; Sirvent N; Vekemans M
    Am J Med Genet C Semin Med Genet; 2016 Sep; 172(3):296-306. PubMed ID: 27474103
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical courses of trisomy 18 (Edwards syndrome) - an update].
    Thiel M; Blanke P; Längler A
    Z Geburtshilfe Neonatol; 2011 Jun; 215(3):109-14. PubMed ID: 21755483
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A very rare entity of diabetes insipidus associated with Edwards syndrome.
    Demir N; Doğan M; Peker E; Bulan K; Tuncer O
    Genet Res (Camb); 2013 Aug; 95(4):130-2. PubMed ID: 24074370
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.