Association of copy number variants with specific ultrasonographically detected fetal anomalies
about
Prevalence of prenatal brain abnormalities in fetuses with congenital heart disease: a systematic reviewArray comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysisGenomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysisClinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.Should we offer prenatal testing for 17q12 microdeletion syndrome to all cases with prenatally diagnosed echogenic kidneys? Prenatal findings in two families with 17q12 microdeletion syndrome and review of the literature.What is the role of the 11- to 14-week ultrasound in women with negative cell-free DNA screening for aneuploidy?Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.A retrospective single centre review of the incidence and prognostic significance of persistent foetal right umbilical vein.Emerging issues in invasive prenatal diagnosis: Safety and competency in the post-NIPT era.Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis.Current controversies in prenatal diagnosis 3: the ethical and counseling implications of new genomic technologies: all pregnant women should be offered prenatal diagnostic genome-wide testing for prenatally identified fetal congenital anomalies.Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction.Association of aberrant right subclavian artery with abnormal karyotype and microarray results.Utility of chromosomal microarray in anomalous fetuses.Prenatal diagnosis by chromosomal microarray analysis.Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with ventricular septal defects by chromosomal microarray-based analysis.17p13.3 quadruplication: a prenatal and postpartum clinical characterization of a copy number variant.Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing
P2860
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P2860
Association of copy number variants with specific ultrasonographically detected fetal anomalies
description
2014 nî lūn-bûn
@nan
2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Association of copy number var ...... cally detected fetal anomalies
@ast
Association of copy number var ...... cally detected fetal anomalies
@en
type
label
Association of copy number var ...... cally detected fetal anomalies
@ast
Association of copy number var ...... cally detected fetal anomalies
@en
prefLabel
Association of copy number var ...... cally detected fetal anomalies
@ast
Association of copy number var ...... cally detected fetal anomalies
@en
P2093
P2860
P1476
Association of copy number var ...... cally detected fetal anomalies
@en
P2093
Jennifer C Donnelly
Julia Zachary
Lawrence D Platt
Ronald J Wapner
William A Grobman
P2860
P356
10.1097/AOG.0000000000000336
P407
P577
2014-07-01T00:00:00Z