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 *

199 related articles for article (PubMed ID: 16032775)

  • 1. The timing of demise in fetuses with trisomy 21 and trisomy 18.
    Won RH; Currier RJ; Lorey F; Towner DR
    Prenat Diagn; 2005 Jul; 25(7):608-11. PubMed ID: 16032775
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fetal pyelectasis: does fetal gender modify the risk of major trisomies?
    Bornstein E; Barnhard Y; Donnenfeld A; Ferber A; Divon MY
    Obstet Gynecol; 2006 Apr; 107(4):877-9. PubMed ID: 16582126
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The identification of risk of spontaneous fetal loss through second-trimester maternal serum screening.
    Huang T; Owolabi T; Summers AM; Meier C; Wyatt PR
    Am J Obstet Gynecol; 2005 Aug; 193(2):395-403. PubMed ID: 16098861
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Screening for trisomy 21 by fetal tricuspid regurgitation, nuchal translucency and maternal serum free beta-hCG and PAPP-A at 11 + 0 to 13 + 6 weeks.
    Falcon O; Auer M; Gerovassili A; Spencer K; Nicolaides KH
    Ultrasound Obstet Gynecol; 2006 Feb; 27(2):151-5. PubMed ID: 16388509
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cesarean section on request at 39 weeks: impact on shoulder dystocia, fetal trauma, neonatal encephalopathy, and intrauterine fetal demise.
    Hankins GD; Clark SM; Munn MB
    Semin Perinatol; 2006 Oct; 30(5):276-87. PubMed ID: 17011400
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Invasive testing for the karyotyping of mid-trimester intrauterine fetal death (IUFD): a pilot study.
    Howarth ES; Konje JC; Healey KA; Duckett DP; Scudamore IW; Taylor DJ
    Prenat Diagn; 2002 Jun; 22(6):453-5. PubMed ID: 12116301
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Acid-base and hematologic values at blood sampling in the evaluation of trisomic fetuses: a case-control study.
    Extermann P; Nicolini U; Rodeck CH
    Obstet Gynecol; 1993 Jun; 81(6):958-62. PubMed ID: 8497363
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The impact of first-trimester screening on AMA patients' uptake of invasive testing.
    Wray AM; Ghidini A; Alvis C; Hodor J; Landy HJ; Poggi SH
    Prenat Diagn; 2005 May; 25(5):350-3. PubMed ID: 15906421
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dichorionic triamniotic triplet pregnancy with monozygotic twins discordant for trisomy 13 after preimplantation genetic screening: case report.
    Taylor DM; Thum MY; Abdalla H
    Fertil Steril; 2008 Nov; 90(5):2017.e5-9. PubMed ID: 18402943
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Outcomes of congenital diaphragmatic hernia: a population-based study in Western Australia.
    Colvin J; Bower C; Dickinson JE; Sokol J
    Pediatrics; 2005 Sep; 116(3):e356-63. PubMed ID: 16140678
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trisomy 21 in one of twin fetuses.
    Heller RH; Palmer LS
    Pediatrics; 1978 Jul; 62(1):52-3. PubMed ID: 150585
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Risk factors for procedure-related fetal losses after mid-trimester genetic amniocentesis.
    Kong CW; Leung TN; Leung TY; Chan LW; Sahota DS; Fung TY; Lau TK
    Prenat Diagn; 2006 Oct; 26(10):925-30. PubMed ID: 16838383
    [TBL] [Abstract][Full Text] [Related]  

  • 13. First-trimester growth patterns of aneuploid fetuses.
    Schemmer G; Wapner RJ; Johnson A; Schemmer M; Norton HJ; Anderson WE
    Prenat Diagn; 1997 Feb; 17(2):155-9. PubMed ID: 9061764
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screening for trisomy 18 by maternal age, fetal nuchal translucency, free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A.
    Kagan KO; Wright D; Maiz N; Pandeva I; Nicolaides KH
    Ultrasound Obstet Gynecol; 2008 Sep; 32(4):488-92. PubMed ID: 18726925
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of trisomy 2 mosaicism: a case report.
    Sifakis S; Velissariou V; Papadopoulou E; Petersen MB; Koumantakis E
    Fetal Diagn Ther; 2004; 19(6):488-90. PubMed ID: 15539872
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A study of oligosaccharide variants of alpha-fetoproteins produced by normal fetuses and fetuses with trisomy 21.
    Yamamoto R; Ohkouchi T; Tabata K; Ebina Y; Watari H; Kudo M; Shimizu K; Satomura S; Minakami H; Sakuragi N
    Acta Obstet Gynecol Scand; 2005 Dec; 84(12):1145-9. PubMed ID: 16305698
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise.
    Chen CP; Chern SR; Chen YY; Wu PC; Town DD; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):430-4. PubMed ID: 23040931
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sex ratios in fetuses and liveborn infants with autosomal aneuploidy.
    Huether CA; Martin RL; Stoppelman SM; D'Souza S; Bishop JK; Torfs CP; Lorey F; May KM; Hanna JS; Baird PA; Kelly JC
    Am J Med Genet; 1996 Jun; 63(3):492-500. PubMed ID: 8737659
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatally detected trisomy 20 mosaicism.
    Robinson WP; McGillivray B; Lewis ME; Arbour L; Barrett I; Kalousek DK
    Prenat Diagn; 2005 Mar; 25(3):239-44. PubMed ID: 15791659
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Frontomaxillary facial angles in screening for trisomy 21 at 14-23 weeks' gestation.
    Sonek J; Borenstein M; Downing C; McKenna D; Neiger R; Croom C; Genrich T; Nicolaides KH
    Am J Obstet Gynecol; 2007 Aug; 197(2):160.e1-5. PubMed ID: 17689634
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.