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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Detalles Bibliográficos
Autores principales: Miny, Peter, Wenzel, Friedel, Tercanli, Sevgi, Filges, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003441/
https://www.ncbi.nlm.nih.gov/pubmed/27605194
http://dx.doi.org/10.3390/microarrays2040304

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003441/
https://www.ncbi.nlm.nih.gov/pubmed/27605194
http://dx.doi.org/10.3390/microarrays2040304

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