dc.date.accessioned | 2022-10-10T03:26:44Z | |
dc.date.accessioned | 2022-10-25T18:53:10Z | |
dc.date.available | 2022-10-10T03:26:44Z | |
dc.date.available | 2022-10-25T18:53:10Z | |
dc.date.created | 2022-10-10T03:26:44Z | |
dc.date.issued | 1991 | |
dc.identifier | https://hdl.handle.net/20.500.12866/12353 | |
dc.identifier | Journal of Medical Genetics | |
dc.identifier | https://doi.org/10.1136/jmg.28.3.205 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/4786824 | |
dc.description.abstract | We report on a girl with mild phenotypic abnormalities and duplication of chromosome 10q11----10q22. The similarities to two previously reported cases with an identical chromosomal aberration provide further support for the delineation of this entity as a specific, clinically recognisable syndrome. | |
dc.language | eng | |
dc.publisher | BMJ Publishing Group | |
dc.relation | urn:issn:1468-6244 | |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.subject | Partial trisomy | |
dc.title | A new case of proximal 10q partial trisomy | |
dc.type | Artículos de revistas | |