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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Galenos Publishing
2022
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| 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 |