Evaluation of Array Comparative genomic Hybridisation in prenatal diagnosis of fetal anomalies: a multicentre cohort study with cost analysis and assessment of patient, health professional and commissioner preferences for array comparative genomic hybridisation

Background: Current pathways for testing fetuses at increased risk of a chromosomal anomaly because of an ultrasound anomaly involve karyotyping after rapid aneuploidy exclusion. Chromosomal microarray (CMA) may detect more clinically significant chromosomal imbalances than karyotyping but evidence...

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Detalhes bibliográficos

Principais autores:	Stephen C Robson, Lyn S Chitty, Stephen Morris, Talitha Verhoef, Gareth Ambler, Diana G Wellesley, Ruth Graham, Claire Leader, Jane Fisher, John A Crolla
Formato:	Artigo
Idioma:	Inglês
Publicado em:	NIHR Journals Library 2017-02-01
coleção:	Efficacy and Mechanism Evaluation
Assuntos:	comparative genomic hybridisation microarray analysis dna copy number variations karyotyping ultrasonography prenatal nuchal translucency measurement congenital abnormalities
Acesso em linha:	https://doi.org/10.3310/eme04010
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