Related references
Note: Only part of the references are listed.Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age
Xiaoqing Wu et al.
JOURNAL OF CLINICAL LABORATORY ANALYSIS (2020)
Prenatal diagnosis by chromosomal microarray analysis
Brynn Levy et al.
FERTILITY AND STERILITY (2018)
Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasia
Zhiyong Zou et al.
PRENATAL DIAGNOSIS (2018)
Impacts of variants of uncertain significance on parental perceptions of children after prenatal chromosome microarray testing
Preeya Desai et al.
PRENATAL DIAGNOSIS (2018)
Fetal congenital heart disease Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome
Meiying Cai et al.
MEDICINE (2018)
The known unknown: the challenges of genetic variants of uncertain significance in clinical practice
Lily Hoffman-Andrews
JOURNAL OF LAW AND THE BIOSCIENCES (2017)
Karyotype versus genomic hybridization for the prenatal diagnosis of chromosomal abnormalities: a metaanalysis
Wilmar Saldarriaga et al.
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY (2015)
Whole-genome array as a first-line cytogenetic test in prenatal diagnosis
M. I. Srebniak et al.
ULTRASOUND IN OBSTETRICS & GYNECOLOGY (2015)
Implementation of high-resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experience
C. Liao et al.
CLINICAL GENETICS (2014)
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
Paul Daniel Brady et al.
GENETICS IN MEDICINE (2014)
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?
D. Ganesamoorthy et al.
BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY (2013)
ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013
Sarah T. South et al.
GENETICS IN MEDICINE (2013)
The Utility of Chromosomal Microarray Analysis in Developmental and Behavioral Pediatrics
Arthur L. Beaudet
CHILD DEVELOPMENT (2013)
Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis
Ronald J. Wapner et al.
NEW ENGLAND JOURNAL OF MEDICINE (2012)
Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound
Lisa G. Shaffer et al.
PRENATAL DIAGNOSIS (2012)
Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities
Malgorzata I. Srebniak et al.
MOLECULAR CYTOGENETICS (2012)
QUADAS-2: A Revised Tool for the Quality Assessment of Diagnostic Accuracy Studies
Penny F. Whiting et al.
ANNALS OF INTERNAL MEDICINE (2011)
Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis
S. C. Hillman et al.
ULTRASOUND IN OBSTETRICS & GYNECOLOGY (2011)
A cytogenetic survey of 14,069 newborn infants
J. L. Hamerton et al.
CLINICAL GENETICS (2010)
Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis
B. H. W. Faas et al.
JOURNAL OF MEDICAL GENETICS (2010)
Paper abstracts of the ISPD 15th international conference on prenatal diagnosis and therapy
PRENATAL DIAGNOSIS (2010)
Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement
David Moher et al.
BMJ-BRITISH MEDICAL JOURNAL (2009)
Fertility preservation in female patients
M Sonmezer et al.
HUMAN REPRODUCTION UPDATE (2004)
Share Paper
