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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.

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Clin Case Rep
Päätekijät: Yan, Xu, Peng, Haiying, Zhang, Changjun
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: John Wiley and Sons Inc. 2021
Aiheet:
Linkit: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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