Array CGH in routine prenatal diagnosis practice: reply letter

被引:0
|
作者
Fioentino, Francesco [1 ]
Caiazzo, Fiorina [1 ]
Napolitano, Stefania [1 ]
Spizzichino, Letizia [1 ]
Bono, Sara [1 ]
Sessa, Mariateresa [1 ]
Nuccitelli, Andrea [1 ]
Biricik, Anil [1 ]
Gordon, Anthony [2 ]
Rizzo, Giuseppe [1 ]
Baldi, Marina [1 ]
机构
[1] GENOMA Mol Genet Lab, I-00198 Rome, Italy
[2] BlueGnome Ltd Cambridge, Cambridge, England
关键词
COMPARATIVE GENOMIC HYBRIDIZATION;
D O I
10.1002/pd.3869
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:711 / 712
页数:2
相关论文
共 50 条
  • [41] Re: ISUOG Practice Guidelines: invasive procedures for prenatal diagnosis Reply
    Ghi, T.
    Sotiriadis, A.
    Raine-Fenning, N.
    [J]. ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2017, 49 (03) : 415 - 417
  • [42] Array CGH in the routine diagnostic work-up of mental retardation
    Heinrich, Uwe
    von Voss, Hubertus
    Rost, Imma
    [J]. LABORATORIUMSMEDIZIN-JOURNAL OF LABORATORY MEDICINE, 2008, 32 (05): : 298 - 307
  • [43] Array technology in prenatal diagnosis
    Zuffardi, Orsetta
    Vetro, Annalisa
    Brady, Paul
    Vermeesch, Joris
    [J]. SEMINARS IN FETAL & NEONATAL MEDICINE, 2011, 16 (02): : 94 - 98
  • [44] Array CGH Substitutes Long Term Culture in CVS Prenatal Testing
    Locher, Maurus
    Traber, Hubert
    Spiegel, Roland
    Achermann, Josef
    [J]. CHROMOSOME RESEARCH, 2013, 21 : S30 - S31
  • [45] 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.
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 158 - 158
  • [46] Application of metaphase and array CGH to preimplantation genetic diagnosis
    Le Caignec, C.
    [J]. CHROMOSOME RESEARCH, 2007, 15 : 12 - 12
  • [47] Early prenatal diagnosis of hemoglobinopathy via celocentesis: Is it ready for use in routine clinical practice?
    Zhao, Yuan
    Li, Dong-Zhi
    [J]. INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 2023, 45 (01) : E17 - E18
  • [48] 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
    [J]. MOLECULAR CYTOGENETICS, 2013, 6
  • [49] 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
    [J]. CHROMOSOME RESEARCH, 2011, 19 : S220 - S221
  • [50] 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
    [J]. CHROMOSOME RESEARCH, 2015, 23 : S115 - S116