相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing
Jing Wang et al.
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY (2018)
Noninvasive prenatal screening or advanced diagnostic testing: caveat emptor
Mark I. Evans et al.
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY (2016)
Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach
Zirui Dong et al.
GENETICS IN MEDICINE (2016)
The Genetics of Microdeletion and Microduplication Syndromes: An Update
Corey T. Watson et al.
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 15 (2014)
New microdeletion and microduplication syndromes: A comprehensive review
Julian Nevado et al.
GENETICS AND MOLECULAR BIOLOGY (2014)
Copy Number Variation Sequencing for Comprehensive Diagnosis of Chromosome Disease Syndromes
Desheng Liang et al.
JOURNAL OF MOLECULAR DIAGNOSTICS (2014)
The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature
Jonathan L. A. Callaway et al.
PRENATAL DIAGNOSIS (2013)
Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis
S. C. Hillman et al.
ULTRASOUND IN OBSTETRICS & GYNECOLOGY (2013)
Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype
G. D'Amours et al.
CLINICAL GENETICS (2012)
Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis
Ronald J. Wapner et al.
NEW ENGLAND JOURNAL OF MEDICINE (2012)
Microdeletion and Microduplication Syndromes
Lisenka E. L. M. Vissers et al.
GENOMIC STRUCTURAL VARIANTS: METHODS AND PROTOCOLS (2012)
Comparing Next-Generation Sequencing and Microarray Technologies in a Toxicological Study of the Effects of Aristolochic Acid on Rat Kidneys
Zhenqiang Su et al.
CHEMICAL RESEARCH IN TOXICOLOGY (2011)
CNV-seq, a new method to detect copy number variation using high-throughput sequencing
Chao Xie et al.
BMC BIOINFORMATICS (2009)
Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization
Trilochan Sahoo et al.
GENETICS IN MEDICINE (2006)
Identification of disease genes by whole genome CGH arrays
LELM Vissers et al.
HUMAN MOLECULAR GENETICS (2005)
Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations
C Le Caignec et al.
JOURNAL OF MEDICAL GENETICS (2005)