Implementation of high-resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experience

Maternal plasma sequencing: a powerful tool towards fetal whole genome recovery

(2013) Elisavet A Papageorgiou et al.   BMC Medicine

0.5 Mb Array as a First-Line Prenatal Cytogenetic Test in Cases without Ultrasound Abnormalities and Its Implementation in Clinical Practice

(2013) Malgorzata I. Srebniak et al.   HUMAN MUTATION

Application of chromosomal microarray in the evaluation of abnormal prenatal findings

(2012) SA Yatsenko et al.   CLINICAL GENETICS

Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis

(2012) Ronald J. Wapner et al.   NEW ENGLAND JOURNAL OF MEDICINE

Non-targeted whole genome 250K SNP array analysis as replacement for karyotyping in fetuses with structural ultrasound anomalies: evaluation of a one-year experience

(2012) Brigitte HW Faas et al.   PRENATAL DIAGNOSIS

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities

(2012) Malgorzata I Srebniak et al.   Molecular Cytogenetics

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype

(2011) G D'Amours et al.   CLINICAL GENETICS

SNP Array Analysis in Constitutional and Cancer Genome Diagnostics – Copy Number Variants, Genotyping and Quality Control

(2011) N. de Leeuw et al.   CYTOGENETIC AND GENOME RESEARCH

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

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

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 in Prenatal Diagnosis: Another Experience

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

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects

(2009) Gurdeep S Sagoo et al.   GENETICS IN MEDICINE

High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings

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

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