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Karyotype versus microarray testing for genetic abnormalities after stillbirth.Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalitiesGenomic microarrays: a technology overview.Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.Prenatal microarray analysis as second-tier diagnostic test: single-center prospective study.The role of DNA microarrays in the evaluation of fetal death.The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies.The introduction of arrays in prenatal diagnosis: a special challenge.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on July 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Copy-number changes in prenatal diagnosis.
@en
Copy-number changes in prenatal diagnosis.
@nl
type
label
Copy-number changes in prenatal diagnosis.
@en
Copy-number changes in prenatal diagnosis.
@nl
prefLabel
Copy-number changes in prenatal diagnosis.
@en
Copy-number changes in prenatal diagnosis.
@nl
P2093
P2860
P356
P1476
Copy-number changes in prenatal diagnosis.
@en
P2093
Gary Fruhman
Ignatia B Van den Veyver
Melissa Strassberg
P2860
P304
P356
10.1586/ERM.11.43
P577
2011-07-01T00:00:00Z