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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.
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| Publicado en: | Clin Case Rep |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2021
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| Materias: | |
| Acceso en línea: | 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 |
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