Literature DB >> 21374637

Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?

The-Hung Bui1, Annalisa Vetro, Orsetta Zuffardi, Lisa G Shaffer.   

Abstract

Mesh：

Year:  2011        PMID： 21374637     DOI： 10.1002/pd.2722

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


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  11 in total

Review 1.  Advances in prenatal screening: the ethical dimension.

Authors:  Antina de Jong; Wybo J Dondorp; Suzanna G M Frints; Christine E M de Die-Smulders; Guido M W R de Wert
Journal:  Nat Rev Genet       Date:  2011-08-18       Impact factor: 53.242

2.  Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.

Authors:  Francesco Fiorentino; Stefania Napoletano; Fiorina Caiazzo; Mariateresa Sessa; Sara Bono; Letizia Spizzichino; Anthony Gordon; Andrea Nuccitelli; Giuseppe Rizzo; Marina Baldi
Journal:  Eur J Hum Genet       Date:  2012-12-05       Impact factor: 4.246

3.  The scope of prenatal diagnosis for women at increased risk for aneuploidies: views and preferences of professionals and potential users.

Authors:  Antina de Jong; Wybo J Dondorp; Anja Krumeich; Julie Boonekamp; Jan M M van Lith; Guido M W R de Wert
Journal:  J Community Genet       Date:  2012-11-09

4.  Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies.

Authors:  Isabel Filges; Anjeung Kang; Vanessa Klug; Friedel Wenzel; Karl Heinimann; Sevgi Tercanli; Peter Miny
Journal:  Mol Cytogenet       Date:  2012-09-17       Impact factor: 2.009

5.  Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH.

Authors:  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
Journal:  Mol Cytogenet       Date:  2013-10-31       Impact factor: 2.009

6.  Design and validation of a pericentromeric BAC clone set aimed at improving diagnosis and phenotype prediction of supernumerary marker chromosomes.

Authors:  Chiara Castronovo; Emanuele Valtorta; Milena Crippa; Sara Tedoldi; Lorenza Romitti; Maria Cristina Amione; Silvana Guerneri; Daniela Rusconi; Lucia Ballarati; Donatella Milani; Enrico Grosso; Pietro Cavalli; Daniela Giardino; Maria Teresa Bonati; Lidia Larizza; Palma Finelli
Journal:  Mol Cytogenet       Date:  2013-10-30       Impact factor: 2.009

7.  Spontaneous abortion and recurrent miscarriage: A comparison of cytogenetic diagnosis in 250 cases.

Authors:  Tae Yeong Choi; Hye Min Lee; Won Kyoung Park; So Yeong Jeong; Hwa Sook Moon
Journal:  Obstet Gynecol Sci       Date:  2014-11-20

8.  Prenatal Diagnosis of Central Nervous System Anomalies by High-Resolution Chromosomal Microarray Analysis.

Authors:  Lijuan Sun; Qingqing Wu; Shi-Wen Jiang; Yani Yan; Xin Wang; Juan Zhang; Yan Liu; Ling Yao; Yuqing Ma; Li Wang
Journal:  Biomed Res Int       Date:  2015-05-12       Impact factor: 3.411

Review 9.  Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?

Authors:  Peter Miny; Friedel Wenzel; Sevgi Tercanli; Isabel Filges
Journal:  Microarrays (Basel)       Date:  2013-12-05

Review 10.  Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature.

Authors:  Paola Evangelidou; Angelos Alexandrou; Maria Moutafi; Marios Ioannides; Pavlos Antoniou; George Koumbaris; Ioannis Kallikas; Voula Velissariou; Carolina Sismani; Philippos C Patsalis
Journal:  Biomed Res Int       Date:  2013-03-04       Impact factor: 3.411
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