Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era

In the age of noninvasive prenatal testing, there is still an important role for invasive prenatal diagnosis, even for chromosomes 13, 18, and 21.

Detalles Bibliográficos
Autores principales: Vervecken, Evy, Blaumeiser, Bettina, Vanderheyden, Tina, Hauspy, Jan, Janssens, Katrien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455455/
https://www.ncbi.nlm.nih.gov/pubmed/32884775
http://dx.doi.org/10.1002/ccr3.2889

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455455/
https://www.ncbi.nlm.nih.gov/pubmed/32884775
http://dx.doi.org/10.1002/ccr3.2889

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