Amniocentesis—When It Is Clear That It Is Not Clear

A fetus identified to be at risk for chromosomal abnormalities may benefit from identification of genetic defects through amniocentesis. Although the risks associated with amniocentesis are considered to be minimal, being an invasive procedure it is not completely without complications. Background a...

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Detalles Bibliográficos
Autores principales: Ciortea, Razvan, Malutan, Andrei Mihai, Bucuri, Carmen Elena, Berceanu, Costin, Rada, Maria Patricia, Ormindean, Cristina Mihaela, Mihu, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9863336/
https://www.ncbi.nlm.nih.gov/pubmed/36675383
http://dx.doi.org/10.3390/jcm12020454

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9863336/
https://www.ncbi.nlm.nih.gov/pubmed/36675383
http://dx.doi.org/10.3390/jcm12020454

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