A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings

An Exploration of Genetic Counselors’ Needs and Experiences with Prenatal Chromosomal Microarray Testing

(2014) Barbara A. Bernhardt et al.   Journal of Genetic Counseling

Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?

(2013) D Ganesamoorthy et al.   BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY

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

(2013) C. Liao et al.   CLINICAL GENETICS

Ethical controversies in prenatal microarray

(2013) Zornitza Stark et al.   CURRENT OPINION IN OBSTETRICS & GYNECOLOGY

A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors

(2013) Paul Daniel Brady et al.   GENETICS IN MEDICINE

How does altering the resolution of chromosomal microarray analysis in the prenatal setting affect the rates of pathological and uncertain findings?

(2013) S. C. Hillman et al.   Journal of Maternal-Fetal & Neonatal Medicine

Controversies in prenatal diagnosis 3: should everyone undergoing invasive testing have a microarray?

(2013) John A. Crolla et al.   PRENATAL DIAGNOSIS

Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years’ clinical application for over 8,700 patients

(2013) Joo Wook Ahn et al.   Molecular Cytogenetics

Implementation of High Resolution Whole Genome Array CGH in the Prenatal Clinical Setting: Advantages, Challenges, and Review of the Literature

(2013) Paola Evangelidou et al.   Biomed Research International

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies

(2012) Fuman Jiang et al.   BMC Medical Genomics

Women’s experiences receiving abnormal prenatal chromosomal microarray testing results

(2012) Barbara A. Bernhardt et al.   GENETICS IN MEDICINE

The introduction of arrays in prenatal diagnosis: A special challenge

(2012) Annalisa Vetro et al.   HUMAN MUTATION

Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis

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

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

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

DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study

(2011) Glenn E. Palomaki et al.   GENETICS IN MEDICINE

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

Application of a target array Comparative Genomic Hybridization to prenatal diagnosis

(2010) Ji Hyeon Park et al.   BMC Medical 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

Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance

(2010) Joo Wook Ahn et al.   Molecular Cytogenetics

De novobalanced chromosome rearrangements in prenatal diagnosis

(2009) Daniela Giardino et al.   PRENATAL DIAGNOSIS

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

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