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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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Bibliographische Detailangaben
Veröffentlicht in:Clin Case Rep
Hauptverfasser: Yan, Xu, Peng, Haiying, Zhang, Changjun
Format: Artigo
Sprache:Inglês
Veröffentlicht: John Wiley and Sons Inc. 2021
Schlagworte:
Online Zugang: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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