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Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?

Microarrays have replaced conventional karyotyping as a first-tier test for unbalanced chromosome anomalies in postnatal cytogenetics mainly due to their unprecedented resolution facilitating the detection of submicroscopic copy number changes at a rate of 10–20% depending on indication for testing....

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Microarrays (Basel)
Prif Awduron: Miny, Peter, Wenzel, Friedel, Tercanli, Sevgi, Filges, Isabel
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: MDPI 2013
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5003441/
https://ncbi.nlm.nih.gov/pubmed/27605194
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/microarrays2040304
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