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.
8. Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities. Grimshaw GM; Szczepura A; Hultén M; MacDonald F; Nevin NC; Sutton F; Dhanjal S Health Technol Assess; 2003; 7(10):1-146. PubMed ID: 12773259 [No Abstract] [Full Text] [Related]
9. Fluorescent in situ hybridization utilization for high-risk prenatal diagnosis: a trade-off among speed, expense, and inherent limitations of chromosome-specific probes. Evans MI; Ebrahim SA; Berry SM; Holzgreve W; Isada NB; Quintero RA; Johnson MP Am J Obstet Gynecol; 1994 Oct; 171(4):1055-7. PubMed ID: 7943069 [TBL] [Abstract][Full Text] [Related]
10. [Isolating fetal cells from maternal blood for noninvasive prenatal diagnosis--from patent to clinical application]. Holzgreve W; Garritsen H; Gänshirt D Z Geburtshilfe Neonatol; 1995; 199(2):47. PubMed ID: 7788576 [No Abstract] [Full Text] [Related]
11. Fluorescent in situ hybridization as an adjunct to conventional cytogenetics. Mark HF Ann Clin Lab Sci; 1994; 24(2):153-63. PubMed ID: 8203823 [TBL] [Abstract][Full Text] [Related]
12. Evaluation of satellited Y chromosome (Yqs) detected during prenatal diagnosis. Haddad BR; Huang Y; Wyandt H; Milunsky A Acta Obstet Gynecol Scand; 1997 Mar; 76(3):281-3. PubMed ID: 9093147 [No Abstract] [Full Text] [Related]
13. Traditional and molecular cytogenetics. Sawyer JR; Johnson MP; Miller OJ J Reprod Med; 1992 Jun; 37(6):485-98. PubMed ID: 1619601 [TBL] [Abstract][Full Text] [Related]
14. [Noninvasive prenatal diagnosis of fetal cells in maternal blood]. Tutschek B; Thomas M; Williamson R; Rodeck CH Gynakologe; 1995 Oct; 28(5):289-301. PubMed ID: 7498825 [No Abstract] [Full Text] [Related]
15. Prenatal detection of chromosome disorders by QF-PCR. Adinolfi M; Sherlock J Lancet; 2001 Sep; 358(9287):1030-1. PubMed ID: 11589930 [No Abstract] [Full Text] [Related]
16. [Advances in rapid prenatal detection of fetal chromosome abnormalities]. Wang J; Cui YX Zhonghua Nan Ke Xue; 2010 Apr; 16(4):359-63. PubMed ID: 20626168 [TBL] [Abstract][Full Text] [Related]
17. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations]. Ulmer R; Pfeiffer RA; Kollert A; Beinder E Z Geburtshilfe Neonatol; 2000; 204(1):1-7. PubMed ID: 10721179 [TBL] [Abstract][Full Text] [Related]
18. Cytogenetics: from aneuploidy to polymorphism. Lin SJ Acta Paediatr Taiwan; 1999; 40(5):297. PubMed ID: 10910535 [No Abstract] [Full Text] [Related]
19. Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities. Lapierre JM; Cacheux V; Collot N; Da Silva F; Hervy N; Rivet D; Romana S; Wiss J; Benzaken B; Aurias A; Tachdjian G Ann Genet; 1998; 41(3):133-40. PubMed ID: 9833066 [TBL] [Abstract][Full Text] [Related]
20. The application of fluorescence in-situ hybridization to prenatal diagnosis. Pergament E Curr Opin Obstet Gynecol; 2000 Apr; 12(2):73-6. PubMed ID: 10813566 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]