Cargando…
A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing
BACKGROUND: Chromosome 18p deletion syndrome is a disease caused by the complete or partial deletion of the short arm of chromosome 18, there were few cases reported about the prenatal diagnosis of 18p deletion syndrome. Noninvasive prenatal testing (NIPT) is widely used in the screening of common f...
| Autores principales: | , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2019
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925888/ https://www.ncbi.nlm.nih.gov/pubmed/31890033 http://dx.doi.org/10.1186/s13039-019-0464-y |