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...

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Detalles Bibliográficos
Autores principales: Zhao, Ganye, Dai, Peng, Gao, Shanshan, Zhao, Xuechao, Wang, Conghui, Liu, Lina, Kong, Xiangdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
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

Internet

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

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