Clinical Features in Patients with Xq23 Microdeletion: A Case Report and Literature Review

• Principais autores: Lu Qin (Autor), Fei-Zhou Zhang (Autor), Jian-Hai Lv (Autor), Lan-Fang Tang (Autor)
• Formato: Livro
• Publicado em: Galenos Yayincilik, 2022-09-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

Xq22.3-q23 microdeletion is a rare genomic disorder. The purpose of this study was to emphasize the correlation between clinical phenotype and genotype of proximal deletion on chromosome Xq22.3-q23. A 5 years old boy had a 671 KB microdeletion on Xq23 by chromosomal microarray analysis, including AM...