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Anomalies of the Genitourinary Tract in Children with 22q11.2 Deletion Syndrome
The 22q11.2 deletion syndrome (22q11.2DS) involves multiple organ systems with variable phenotypic expression. Genitourinary tract abnormalities have been noted to be present in up to 30–40% of patients. At our institution, an internationally recognized, comprehensive and multidisciplinary 22q11.2DS...
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| Vydáno v: | Am J Med Genet A |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6491205/ https://ncbi.nlm.nih.gov/pubmed/30582277 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.61020 |
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