PCR vs karyotype for CVS and amniocentesis—the experience at one tertiary fetal medicine unit

PURPOSE: Despite the rise of non-invasive screening tests for fetal aneuploidy, invasive testing during pregnancy remains the definitive diagnostic tool for fetal genetic anomalies. Results are rapidly available with polymerase chain reaction (PCR) tests, but cases have been reported whereby initial...

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Detalles Bibliográficos
Autores principales: Finnegan, Catherine, Smyth, Suzanne, Smith, Orla, Flood, Karen, Dalrymple, Jane, Breathnach, Fionnuala M., Malone, Fergal D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135887/
https://www.ncbi.nlm.nih.gov/pubmed/34283385
http://dx.doi.org/10.1007/s11845-021-02715-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135887/
https://www.ncbi.nlm.nih.gov/pubmed/34283385
http://dx.doi.org/10.1007/s11845-021-02715-y

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