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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.
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
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 |
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author | Vervecken, Evy Blaumeiser, Bettina Vanderheyden, Tina Hauspy, Jan Janssens, Katrien |
author_facet | Vervecken, Evy Blaumeiser, Bettina Vanderheyden, Tina Hauspy, Jan Janssens, Katrien |
author_sort | Vervecken, Evy |
collection | PubMed |
description | In the age of noninvasive prenatal testing, there is still an important role for invasive prenatal diagnosis, even for chromosomes 13, 18, and 21. |
format | Online Article Text |
id | pubmed-7455455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74554552020-09-02 Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era Vervecken, Evy Blaumeiser, Bettina Vanderheyden, Tina Hauspy, Jan Janssens, Katrien Clin Case Rep Case Reports In the age of noninvasive prenatal testing, there is still an important role for invasive prenatal diagnosis, even for chromosomes 13, 18, and 21. John Wiley and Sons Inc. 2020-05-13 /pmc/articles/PMC7455455/ /pubmed/32884775 http://dx.doi.org/10.1002/ccr3.2889 Text en © 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Vervecken, Evy Blaumeiser, Bettina Vanderheyden, Tina Hauspy, Jan Janssens, Katrien Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era |
title | Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era |
title_full | Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era |
title_fullStr | Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era |
title_full_unstemmed | Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era |
title_short | Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era |
title_sort | terminal deletion of chromosome 13 in a fetus with normal nipt: the added value of invasive prenatal diagnosis in the nipt era |
topic | Case Reports |
url | 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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