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A case report of chromosome 17q22‐qter trisomy with distinct clinical presentation and review of the literature
Terminal 17q trisomy is very rare but a recognizable genetic syndrome. The majority of cases reported are inherited from a balanced translocation carrier. This syndrome involves many organs and the severity ranges from mild to severe depending on the size of the 17q gain.
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5889218/ https://www.ncbi.nlm.nih.gov/pubmed/29636925 http://dx.doi.org/10.1002/ccr3.1298 |