Carregant...
Prenatal diagnosis of a de novo trisomy 20p detected by noninvasive prenatal testing
Prenatal diagnosis of trisomy 20p seems to be difficult, considering the capacity of ultrasound to detect mild dysmorphic. NIPT has good performance in detecting fetal trisomy 20p combined with low coverage WGS and karyotype analysis.
Guardat en:
| Publicat a: | Clin Case Rep |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2021
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8077397/ https://ncbi.nlm.nih.gov/pubmed/33936600 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.3587 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|