Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis
about
Clinical utility of array comparative genomic hybridisation in prenatal setting.Declining invasive prenatal diagnostic procedures: A comparison of tertiary hospital and national data from 2012 to 2015.Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPT.Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.Cell-free DNA testing of an extended range of chromosomal anomalies: clinical experience with 6,388 consecutive cases.Population-based impact of noninvasive prenatal screening on screening and diagnostic testing for fetal aneuploidy.Principles of first trimester screening in the age of non-invasive prenatal diagnosis: screening for chromosomal abnormalities.Recurrent increased nuchal translucency: a first trimester presentation of familial 13p satellite deletion.Neuropsychiatric aspects of 22q11.2 deletion syndrome: considerations in the prenatal setting.The added value of detailed early anomaly scan in fetuses with increased nuchal translucency.Cut-off value of nuchal translucency as indication for chromosomal microarray analysis.Re: Cut-off value of nuchal translucency as indication for chromosomal microarray analysis. I. Maya, S. Yacobson, S. Kahana, J. Yeshaya, T. Tenne, I. Agmon-Fishman, L. Cohen-Vig, M. Shohat, L. Basel-Vanagaite and R. Sharony. Ultrasound Obstet GynecoThe effect of progesterone use in the first trimester on fetal nuchal translucency.Current controversies in prenatal diagnosis 3: is there still a value in a nuchal translucency screening ultrasound in conjunction with maternal plasma non-invasive cell-free DNA testing?ISUOG Practice Guidelines: invasive procedures for prenatal diagnosis.Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
P2860
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P2860
Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis
description
2015 nî lūn-bûn
@nan
2015 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Genomic microarray in fetuses ...... matic review and meta-analysis
@ast
Genomic microarray in fetuses ...... matic review and meta-analysis
@en
Genomic microarray in fetuses ...... matic review and meta-analysis
@nl
type
label
Genomic microarray in fetuses ...... matic review and meta-analysis
@ast
Genomic microarray in fetuses ...... matic review and meta-analysis
@en
Genomic microarray in fetuses ...... matic review and meta-analysis
@nl
prefLabel
Genomic microarray in fetuses ...... matic review and meta-analysis
@ast
Genomic microarray in fetuses ...... matic review and meta-analysis
@en
Genomic microarray in fetuses ...... matic review and meta-analysis
@nl
P2093
P2860
P31
P3181
P356
P1476
Genomic microarray in fetuses ...... matic review and meta-analysis
@en
P2093
F A R Jansen
Y J Blumenfeld
P2860
P304
P3181
P356
10.1002/UOG.14880
P407
P577
2015-12-01T00:00:00Z