Referral patterns for microarray testing in prenatal diagnosis

Evolving applications of microarray analysis in prenatal diagnosis

(2011) Melissa S Savage et al.   CURRENT OPINION IN OBSTETRICS & GYNECOLOGY

A copy number variation morbidity map of developmental delay

(2011) Gregory M Cooper et al.   NATURE GENETICS

Prenatal BACs-on-Beads™: a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosis

(2011) F. Vialard et al.   PRENATAL DIAGNOSIS

Rapid and novel prenatal molecular assay for detecting aneuploidies and microdeletion syndromes

(2011) Susan J. Gross et al.   PRENATAL DIAGNOSIS

The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes

(2011) Lisa G. Shaffer et al.   PRENATAL DIAGNOSIS

Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases

(2011) Sang-Jin Park et al.   Molecular Cytogenetics

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

Evaluation of Array Comparative Genomic Hybridization for Genetic Analysis of Chorionic Villus Sampling from Pregnancy Loss in Comparison to Karyotyping and Multiplex Ligation-Dependent Probe Amplification

(2010) Maitreyee Deshpande et al.   Genetic Testing and Molecular Biomarkers

Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

(2010) Melanie Manning et al.   GENETICS IN MEDICINE

Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss

(2010) E. Rajcan-Separovic et al.   HUMAN REPRODUCTION

Array Comparative Genomic Hybridization Findings in a Cohort Referred for an Autism Evaluation

(2010) G. Bradley Schaefer et al.   JOURNAL OF CHILD NEUROLOGY

Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis

(2010) B. H. W. Faas et al.   JOURNAL OF MEDICAL GENETICS

Genome-Wide Oligonucleotide Array Comparative Genomic Hybridization for Etiological Diagnosis of Mental Retardation

(2010) Bixia Xiang et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

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 comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples

(2009) Björn Menten et al.   BMC Medical Genetics

Array Comparative Genomic Hybridization in Prenatal Diagnosis: Another Experience

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

High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings

(2009) M Tyreman et al.   JOURNAL OF MEDICAL GENETICS

Genomic changes detected by array CGH in human embryos with developmental defects

(2009) E. Rajcan-Separovic et al.   MOLECULAR HUMAN REPRODUCTION

ACOG Committee Opinion No. 446: Array Comparative Genomic Hybridization in Prenatal Diagnosis

(2009)   OBSTETRICS AND GYNECOLOGY

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

Array comparative genomic hybridization in global developmental delay

(2008) M.I. Shevell et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Emerging themes and new challenges in defining the role of structural variation in human disease

(2008) Andrew J. Sharp   HUMAN MUTATION

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

(2008) Lisa G. Shaffer et al.   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