Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases-Reference-Cited by-同舟云学术

Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases

Published:2011-10-28 Issue:13 Volume:31 Page:1270-1282
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Fiorentino Francesco¹,Caiazzo Fiorina¹,Napolitano Stefania¹,Spizzichino Letizia¹,Bono Sara¹,Sessa Mariateresa¹,Nuccitelli Andrea¹,Biricik Anil¹,Gordon Anthony²,Rizzo Giuseppe¹,Baldi Marina¹

Affiliation:

1. ‘GENOMA’ Molecular Genetics Laboratory; Via Po 102 00198 Rome Italy

2. Bluegnome Ltd; Cambridge CB22 5LD UK

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.2884/fullpdf

Reference47 articles.

1. Array comparative genomic hybridisation in prenatal diagnosis;ACOG Committee;Obstet Gynecol,2009

2. Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance;Ahn;Mol Cytogenet,2010

3. Detection of low-level mosaicism by array CGH in routine diagnostic specimens;Ballif;Am J Med Genet A,2006

4. Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGH;Ballif;Genet Med,2007

5. Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?;Bejjani;Am J Med Genet A,2005

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