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.

Detalles Bibliográficos
Autores principales: Yan, Xu, Peng, Haiying, Zhang, Changjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077397/
https://www.ncbi.nlm.nih.gov/pubmed/33936600
http://dx.doi.org/10.1002/ccr3.3587

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077397/
https://www.ncbi.nlm.nih.gov/pubmed/33936600
http://dx.doi.org/10.1002/ccr3.3587

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