Published 2020
| Version v1
Publication
Prenatal Diagnosis of an Uncommon 48,XX,+18+21 Karyotype in a Fetus With Malformations Typical of Both Trisomies
Additional details
- URL
- http://hdl.handle.net/11567/1036477
- URN
- urn:oai:iris.unige.it:11567/1036477
- Origin repository
- UNIGE