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...

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Main Authors: Lu Qin (Author), Fei-Zhou Zhang (Author), Jian-Hai Lv (Author), Lan-Fang Tang (Author)
Format: Book
Published: Galenos Yayincilik, 2022-09-01T00:00:00Z.
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