Accuracy of cytogenetic findings on chorionic villus sampling (CVS)--diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centres contributing to EUCROMIC 1986-1992
about
Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic lociReview: cell-free fetal DNA in the maternal circulation as an indication of placental health and diseaseNoninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy managementBACs-on-Beads technology: a reliable test for rapid detection of aneuploidies and microdeletions in prenatal diagnosisChromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis.Unexplained False Negative Results in Noninvasive Prenatal Testing: Two Cases Involving Trisomies 13 and 18.The importance of screening and prenatal diagnosis in the identification of the numerical chromosomal abnormalitiesCell-free fetal DNA in the maternal circulation originates from the cytotrophoblast: proof from an unique case.Integration of noninvasive DNA testing for aneuploidy into prenatal care: what has happened since the rubber met the road?Non-invasive Prenatal Testing: Technologies, Clinical Assays and Implementation Strategies for Women's Healthcare Practitioners.Fetoplacental discrepancy with normal karyotype in amniotic fluid and two different cell lines in placentaA retrospective and theoretical evaluation of rapid methods for detecting chromosome abnormalities and their implications on genetic counseling based on a series of 3868 CVS diagnoses.Detection of chromosome aneuploidies in chorionic villus samples by multiplex ligation-dependent probe amplification.Noninvasive fetal genome sequencing: a primerQuantitative fluorescent polymerase chain reaction for rapid prenatal diagnosis of fetal aneuploidies in chorionic villus sampling in a single institution.The accuracy of chromosomal microarray testing for identification of embryonic mosaicism in human blastocysts.Copy-number changes in prenatal diagnosis.Incidence of placental mosaicism leading to discrepant results between QF-PCR and karyotyping in 22,825 chorionic villus samples.Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.Non-invasive prenatal testing for aneuploidy: current status and future prospects.Clinical implementation of NIPT - technical and biological challenges.Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberration.Discordant non-invasive prenatal testing (NIPT) - a systematic review.Natural Frequencies Do Not Foster Public Understanding of Medical Test Results.Fetoplacental discrepancy involving structural abnormalities of chromosome 8 detected by prenatal diagnosis.Trisomy 12 mosaicism confirmed in multiple organs from a liveborn child.A rare case of a mosaic unbalanced translocation after chorionic villous sampling.Prenatal microarray analysis as second-tier diagnostic test: single-center prospective study.Discordant prenatal diagnosis of trisomy 21 due to mosaic structural rearrangements of chromosome 21.Sex chromosome aneuploidy detection by noninvasive prenatal testing: helpful or hazardous?A comparison of in vitro culture of fetal nucleated erythroblasts from fetal chorionic villi and maternal peripheral blood for noninvasive prenatal diagnosis.Prenatal diagnosis of chromosomal mosaicism in over 1600 cases using array comparative genomic hybridization as a first line test.QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first-trimester prenatal diagnoses.Structural chromosomal abnormalities detected during CVS analysis and their role in the prenatal ascertainment of cryptic subtelomeric rearrangementsThe structure of medical decisions: uncertainty, probability and risk in five common choice situations
P2860
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P2860
Accuracy of cytogenetic findings on chorionic villus sampling (CVS)--diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centres contributing to EUCROMIC 1986-1992
description
1997 nî lūn-bûn
@nan
1997 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Accuracy of cytogenetic findin ...... ributing to EUCROMIC 1986-1992
@ast
Accuracy of cytogenetic findin ...... ributing to EUCROMIC 1986-1992
@en
Accuracy of cytogenetic findin ...... ributing to EUCROMIC 1986-1992
@nl
type
label
Accuracy of cytogenetic findin ...... ributing to EUCROMIC 1986-1992
@ast
Accuracy of cytogenetic findin ...... ributing to EUCROMIC 1986-1992
@en
Accuracy of cytogenetic findin ...... ributing to EUCROMIC 1986-1992
@nl
prefLabel
Accuracy of cytogenetic findin ...... ributing to EUCROMIC 1986-1992
@ast
Accuracy of cytogenetic findin ...... ributing to EUCROMIC 1986-1992
@en
Accuracy of cytogenetic findin ...... ributing to EUCROMIC 1986-1992
@nl
P2860
P1433
P1476
Accuracy of cytogenetic findin ...... ributing to EUCROMIC 1986-1992
@en
P2093
J M Hahnemann
L O Vejerslev
P2860
P304
P356
10.1002/(SICI)1097-0223(199709)17:9<801::AID-PD153>3.0.CO;2-E
P407
P577
1997-09-01T00:00:00Z