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Autor:
Mihu, Razvan Ciortea, Andrei Mihai Malutan, Carmen Elena Bucuri, Costin Berceanu, Maria Patricia Rada, Cristina Mihaela Ormindean, Dan
Publikováno v:
Journal of Clinical Medicine; Volume 12; Issue 2; Pages: 454
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::cde55a81b9a29b3edbb3da6e31816ec4
