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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....
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| Vydáno v: | Microarrays (Basel) |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2013
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| Témata: | |
| On-line přístup: | 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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