Prenatal diagnosis of de novo monosomy 18p deletion syndrome by chromosome microarray analysis: Three case reports

RATIONALE: Monosomy 18p deletion syndrome refers to a rare chromosomal disorder resulting from the part deletion of the short arm of chromosome 18. Prenatal diagnosis of de novo 18p deletion syndrome is a challenge due to its low incidence and untypical prenatal clinical presentation. PATIENT CONCER...

Descripción completa

Detalles Bibliográficos
Autores principales: Qi, Hong, Zhu, Jianjiang, Zhang, Shaoqin, Cai, Lirong, Wen, Xiaohui, Zeng, Wen, Tang, Guodong, Luo, Yao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456123/
https://www.ncbi.nlm.nih.gov/pubmed/30946338
http://dx.doi.org/10.1097/MD.0000000000015027

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456123/
https://www.ncbi.nlm.nih.gov/pubmed/30946338
http://dx.doi.org/10.1097/MD.0000000000015027

Ejemplares similares