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: | , , , |
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| Format: | Book |
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Galenos Yayincilik,
2022-09-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |