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 *

156 related articles for article (PubMed ID: 10694684)

  • 1. Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study.
    Lapierre JM; Cacheux V; Luton D; Collot N; Oury JF; Aurias A; Tachdjian G
    Prenat Diagn; 2000 Feb; 20(2):123-31. PubMed ID: 10694684
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosome analysis of uncultured amniocytes by comparative genomic hybridization in early amniocentesis.
    Ketupanya A; Aranyakasemsuk N; Tocharoentanaphol C; Vuthiwong C
    J Med Assoc Thai; 2005 Nov; 88 Suppl 3():S1-6. PubMed ID: 16862671
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
    Zhang YP; Wu JP; Li XT; Lei CX; Xu JZ; Yin M
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH).
    Witters I; Devriendt K; Legius E; Matthijs G; Van Schoubroeck D; Van Assche FA; Fryns JP
    Prenat Diagn; 2002 Jan; 22(1):29-33. PubMed ID: 11810646
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
    Wang J; Chen L; Zhou C; Wang L; Xie H; Xiao Y; Zhu H; Hu T; Zhang Z; Zhu Q; Liu Z; Liu S; Wang H; Xu M; Ren Z; Yu F; Cram DS; Liu H
    Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Defining the role of fluorescence in situ hybridization on uncultured amniocytes for prenatal diagnosis of aneuploidies.
    D'Alton ME; Malone FD; Chelmow D; Ward BE; Bianchi DW
    Am J Obstet Gynecol; 1997 Apr; 176(4):769-74; discussion 774-6. PubMed ID: 9125600
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. 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]  

  • 9. [Prenatal diagnosis of common chromosomal aneuploidies on uncultured amniotic fluid cells by fluorescence in situ hybridization].
    Xiao HM; Tan YQ; Li LY; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):608-10. PubMed ID: 15583993
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A prospective comparative study on fluorescence in situ hybridization (FISH) of uncultured amniocytes and standard karyotype analysis.
    Eiben B; Trawicki W; Hammans W; Goebel R; Epplen JT
    Prenat Diagn; 1998 Sep; 18(9):901-6. PubMed ID: 9793971
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Value of detection of cell-free fetal DNA in maternal plasma in the prenatal diagnosis of chromosomal abnormalities].
    Wang SJ; Gao ZY; Lu YP; Li YL; You YQ; Zhang LW; Wang LX; Xu H
    Zhonghua Fu Chan Ke Za Zhi; 2012 Nov; 47(11):808-12. PubMed ID: 23302119
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Application of fluorescence in situ hybridization to prenatal diagnosis of aneuploidy in 110 uncultured amniotic fluid samples].
    Liu H; Liao C; Huang YN; Pan M; Yi CX; Yuan SM; Hu SY; Zhong HZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):453-6. PubMed ID: 20677157
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo-fetal development anomalies.
    Tabet AC; Aboura A; Dauge MC; Audibert F; Coulomb A; Batallan A; Couturier-Turpin MH; Feldmann G; Tachdjian G
    Prenat Diagn; 2001 Aug; 21(8):613-8. PubMed ID: 11536256
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid.
    Miura S; Miura K; Masuzaki H; Miyake N; Yoshiura KI; Sosonkina N; Harada N; Shimokawa O; Nakayama D; Yoshimura S; Matsumoto N; Niikawa N; Ishimaru T
    J Hum Genet; 2006; 51(5):412-417. PubMed ID: 16622586
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Rapid detection of the most common chromosomal aneuploidies in the second-trimester amniotic fluid using QF-PCR].
    Švecová I; Burjanivová T; Kršiaková J; Lasabová Z; Biringer K; Kapustová I; Móricová P; Danko J
    Ceska Gynekol; 2013 Aug; 78(4):373-8. PubMed ID: 24040987
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: a prospective study.
    Spathas DH; Divane A; Maniatis GM; Ferguson-Smith ME; Ferguson-Smith MA
    Prenat Diagn; 1994 Nov; 14(11):1049-54. PubMed ID: 7877952
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Use of a DNA method, QF-PCR, in the prenatal diagnosis of fetal aneuploidies.
    Langlois S; Duncan A; ;
    J Obstet Gynaecol Can; 2011 Sep; 33(9):955-960. PubMed ID: 21923994
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridization.
    Christensen B; Bryndorf T; Philip J; Lundsteen C; Hansen W
    Prenat Diagn; 1992 Apr; 12(4):241-50. PubMed ID: 1614982
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Application of fluorescence in situ hybridization in prenatal diagnosis of chromosomal abnormalities in uncultured amniocytes: a multi-center study].
    Wang SY; Huang XH; Jia CW; Li Y; Ren GQ
    Zhonghua Fu Chan Ke Za Zhi; 2009 Jul; 44(7):492-5. PubMed ID: 19957546
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.