dc.date.accessioned2022-10-10T03:26:44Z
dc.date.accessioned2022-10-25T18:53:10Z
dc.date.available2022-10-10T03:26:44Z
dc.date.available2022-10-25T18:53:10Z
dc.date.created2022-10-10T03:26:44Z
dc.date.issued1991
dc.identifierhttps://hdl.handle.net/20.500.12866/12353
dc.identifierJournal of Medical Genetics
dc.identifierhttps://doi.org/10.1136/jmg.28.3.205
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4786824
dc.description.abstractWe 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.languageeng
dc.publisherBMJ Publishing Group
dc.relationurn:issn:1468-6244
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectPartial trisomy
dc.titleA new case of proximal 10q partial trisomy
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución