Array CGH Substitutes Long Term Culture in CVS Prenatal Testing

被引:0
|
作者
Locher, Maurus [1 ]
Traber, Hubert [1 ]
Spiegel, Roland [1 ]
Achermann, Josef [1 ]
机构
[1] Genet AG, Human Genet, Zurich, Switzerland
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
O15
引用
收藏
页码:S30 / S31
页数:2
相关论文
共 50 条
  • [41] Long-term stimulation of mouse hippocampal slice culture on microelectrode array
    van Bergen, A
    Papanikolaou, T
    Schuker, A
    Möller, A
    Schlosshauer, B
    BRAIN RESEARCH PROTOCOLS, 2003, 11 (02): : 123 - 133
  • [42] Applications of array CGH testing to clinical cytogenetics - What should we be doing?
    Brothman, A. R.
    Aston, E.
    Whitby, H.
    South, S.
    Issa, B.
    Xu, J.
    Chen, Z.
    Pickering, D. L.
    Sanger, W.
    Williams, M.
    CYTOGENETIC AND GENOME RESEARCH, 2007, 116 (04)
  • [43] Retrospective investigation of array-CGH prenatal diagnosis at Geneva Hospital: a cohort of 626 pregnancies
    Gimelli, S.
    Stathaki, E.
    Kremer, V.
    Weber, B. Martinez de Tejada
    Extermann, P.
    Pellegrinelli, J.
    Billieux, M.
    Eperon, I.
    Mirlesse, V.
    Heggel-Hort, B.
    Plaschy, B.
    Von Kanel, T.
    Fokstuen, S.
    Robyr, R.
    Ranza, E.
    Antonarakis, S.
    Abramowicz, M.
    Sloan-Bena, F.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 578 - 578
  • [44] The Controversial Molecular Turn in Prenatal Diagnosis CGH-array Clinical Approaches and Biomedical Platforms
    Turrini, Mauro
    TECNOSCIENZA-ITALIAN JOURNAL OF SCIENCE & TECHNOLOGY STUDIES, 2014, 5 (01): : 115 - 139
  • [45] Do we really need to know fetal gender for array-CGH in prenatal diagnosis?
    Ferreira, Susana I.
    Val, Mariana
    Pires, Luis M.
    Lavoura, Nuno
    Melo, Joana B.
    Carreira, Isabel M.
    MEDICINE, 2020, 99 (09)
  • [46] Retrospective analysis of prenatal samples with unbalanced structural rearrangements using BAC array-CGH
    Maggi, F.
    De Toffol, S.
    Pecoraro, D.
    Raussi, H.
    Ollikka, P.
    Grimi, B.
    Milani, S.
    Borsatti, A.
    Simoni, G.
    Grati, F.
    CHROMOSOME RESEARCH, 2009, 17 : 184 - 184
  • [47] Prenatal Testing and Disability: A Truce in the Culture Wars?
    Dresser, Rebecca
    HASTINGS CENTER REPORT, 2009, 39 (03) : 7 - 8
  • [48] A prenatal missed diagnosed case of submicroscopic chromosomal abnormalities by karyotyping: the clinical utility of array-based CGH in prenatal diagnostics
    Yin, Aihua
    Lu, Jian
    Liu, Chang
    Guo, Li
    Wu, Jing
    Mai, Mingqin
    Zhong, Yanfang
    Zhang, Xiaozhuang
    MOLECULAR CYTOGENETICS, 2014, 7
  • [49] A prenatal missed diagnosed case of submicroscopic chromosomal abnormalities by karyotyping: the clinical utility of array-based CGH in prenatal diagnostics
    Aihua Yin
    Jian Lu
    Chang Liu
    Li Guo
    Jing Wu
    Mingqin Mai
    Yanfang Zhong
    Xiaozhuang Zhang
    Molecular Cytogenetics, 7
  • [50] Clinical experience of unexpected findings in prenatal array testing
    Joosten, Marieke
    Diderich, Karin E. M.
    Van Opstal, Diane
    Govaerts, Lutgarde C. P.
    Riedijk, Sam R.
    Prinsen, A. Krista E.
    De Vries, Femke A. T.
    Go, Attie T. J. I.
    Galjaard, Robert-Jan H.
    Srebniak, Malgorzata I.
    BIOMARKERS IN MEDICINE, 2016, 10 (08) : 831 - 840