Tailoring array CGH for prenatal diagnosis, early experience at CUHK.

被引:0
|
作者
Choy, Richard K. W. [1 ,2 ]
机构
[1] Chinese Univ Hong Kong, Dept Obstet & Gynaecol, Hong Kong, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, Hong Kong, Hong Kong, Peoples R China
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
引用
收藏
页码:27 / 28
页数:2
相关论文
共 50 条
  • [41] Prenatal array CGH: towards a more appropriate and targeted clinical use
    Gentile, M.
    Pansini, A.
    Ficarella, R.
    Buonadonna, A. L.
    Zambetti, P.
    Moretti, M.
    Volpe, P.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 158 - 158
  • [42] Array CGH Substitutes Long Term Culture in CVS Prenatal Testing
    Locher, Maurus
    Traber, Hubert
    Spiegel, Roland
    Achermann, Josef
    CHROMOSOME RESEARCH, 2013, 21 : S30 - S31
  • [43] EXPERIENCE IN PRENATAL DIAGNOSIS
    AVENDANO, I
    ASPILLAGA, M
    ARCHIVOS DE BIOLOGIA Y MEDICINA EXPERIMENTALES, 1980, 13 (01): : 125 - 125
  • [44] Application of metaphase and array CGH to preimplantation genetic diagnosis
    Le Caignec, C.
    CHROMOSOME RESEARCH, 2007, 15 : 12 - 12
  • [45] Prenatal Array CGH: initial experience of a regional fetal medicine centre shows high rates of suboptimal and failed samples
    Walker, L.
    Cohen, K.
    BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2016, 123 : 65 - 65
  • [46] Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH
    Manolakos, Emmanouil
    Kefalas, Konstantinos
    Vetro, Annalisa
    Oikonomidou, Eirini
    Daskalakis, George
    Psara, Natasa
    Siomou, Elisa
    Papageorgiou, Elena
    Sevastopoulou, Eirini
    Konstantinidou, Anastasia
    Vrachnis, Nikolaos
    Thomaidis, Loretta
    Zuffardi, Orsetta
    Papoulidis, Ioannis
    MOLECULAR CYTOGENETICS, 2013, 6
  • [47] Clinical application of whole-genome array-CGH during prenatal diagnosis: study of 25 selected pregnancies
    Cardarelli, Laura
    Nalesso, Elisa
    Gomirato, Sara
    Michelotto, Lisa
    Marchioro, Katia
    Cellamare, Angelo
    Duca, Manuela
    Zavan, Barbara
    Abatangelo, Giovanni
    CHROMOSOME RESEARCH, 2011, 19 : S220 - S221
  • [48] Prenatal diagnosis of Simpson-Golabi-Behmel Syndrome Type 1 by array CGH in a second trimester twin pregnancy
    Morotti, Denise
    Motta, Silvia
    Baccarin, Marco
    Silipigni, Rosamaria
    Boito, Simona
    Natacci, Federica
    Guerneri, Silvana
    CHROMOSOME RESEARCH, 2015, 23 : S115 - S116
  • [49] Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH
    Emmanouil Manolakos
    Konstantinos Kefalas
    Annalisa Vetro
    Eirini Oikonomidou
    George Daskalakis
    Natasa Psara
    Elisa Siomou
    Elena Papageorgiou
    Eirini Sevastopoulou
    Anastasia Konstantinidou
    Nikolaos Vrachnis
    Loretta Thomaidis
    Orsetta Zuffardi
    Ioannis Papoulidis
    Molecular Cytogenetics, 6
  • [50] Comparison of variants of uncertain significance (VOUS) using different array CGH resolution platforms-implication in prenatal diagnosis
    Oikonomidou, E.
    Efstathiou, G.
    Malamaki, C.
    Darmani, E.
    Arampatzi, A.
    Zavlanos, A.
    Vittas, S.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 117 - 118