Cargando…

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

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Qin, Lu, Zhang, Fei-Zhou, Lv, Jian-Hai, Tang, Lan-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9422909/
https://www.ncbi.nlm.nih.gov/pubmed/33535730
http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0100