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Detection of 21q11.2‐q22.11 deletions in a fetus by NIPT
BACKGROUND: Non‐invasive prenatal testing (NIPT) is extensively used in the detection of fetal trisomies 21, 18, and 13, which is promptly becoming a common clinical practice. Concerned about the clinical application of non‐invasive detection of the fetal autosomal duplications or deletion. CASE PRE...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6818560/ https://www.ncbi.nlm.nih.gov/pubmed/30666717 http://dx.doi.org/10.1002/jcla.22711 |