Karyotype versus genomic hybridization for the prenatal diagnosis of chromosomal abnormalities: a metaanalysis

Author:

Saldarriaga Wilmar,García-Perdomo Herney AndrésORCID,Arango-Pineda Johanna,Fonseca Javier

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference29 articles.

1. Technique modifications for reducing the risks from amniocentesis or chorionic villus sampling;Mujezinovic;Cochrane Database Syst Rev,2012

2. Prenatal maternal blood screening for the detection of fetal chromosomal abnormalities: clinical importance of the rate of false positives;Alvarez-Nava;Invest Clin,2003

3. Diagnóstico prenatal y array-CGH II: gestaciones de bajo riesgo;Querejeta;Diagnostico Prenat,2012

4. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies;Miller;Am J Hum Genet,2010

5. Value for money? Array genomic hybridization for diagnostic testing for genetic causes of intellectual disability;Regier;Am J Hum Genet,2010

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