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

Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies

(2012) C-N Lee et al.   BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY

The introduction of arrays in prenatal diagnosis: A special challenge

(2012) Annalisa Vetro et al.   HUMAN MUTATION

Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing

(2012) George McGillivray et al.   PRENATAL DIAGNOSIS

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature

(2012) Amy Breman et al.   PRENATAL DIAGNOSIS

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow

(2011) Malgorzata Srebniak et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Copy-number changes in prenatal diagnosis

(2011) Melissa Strassberg et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis

(2011) Lluís Armengol et al.   HUMAN GENETICS

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

(2011) Francesco Fiorentino et al.   PRENATAL DIAGNOSIS

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

(2011) The-Hung Bui et al.   PRENATAL DIAGNOSIS

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

(2010) David T. Miller et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting

(2010) Idit Maya et al.   PRENATAL DIAGNOSIS

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis

(2010) S. C. Hillman et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY

Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands

(2009) Ron Hochstenbach et al.   European Journal of Medical Genetics

Array Comparative Genomic Hybridization in Prenatal Diagnosis: Another Experience

(2009) F. Vialard et al.   FETAL DIAGNOSIS AND THERAPY

Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray

(2009) Justine Coppinger et al.   PRENATAL DIAGNOSIS

Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype

(2009) Linda Kleeman et al.   PRENATAL DIAGNOSIS

Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives

(2008) Sandra Darilek et al.   GENETICS IN MEDICINE

Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens

(2008) Lisa G. Shaffer et al.   PRENATAL DIAGNOSIS

Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH

(2008) Weimin Bi et al.   PRENATAL DIAGNOSIS

Current controversies in prenatal diagnosis 3: for prenatal diagnosis, should we offer less or more than metaphase karyotyping?

(2008) Caroline M. Ogilvie et al.   PRENATAL DIAGNOSIS

High-resolution array genomic hybridization in prenatal diagnosis

(2008) J. M. Friedman   PRENATAL DIAGNOSIS

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

(2008) Ignatia B. Van den Veyver et al.   PRENATAL DIAGNOSIS