A new case of proximal 10q partial trisomy

dc.contributor.author	de Michelena, M
dc.contributor.author	Campos, P
dc.date.accessioned	2022-10-10T03:26:12Z
dc.date.available	2022-10-10T03:26:12Z
dc.date.issued	1991
dc.identifier.uri	https://hdl.handle.net/20.500.12866/12339
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.	en_US
dc.language.iso	eng
dc.publisher	BMJ Publishing Group
dc.relation.ispartofseries	Journal of Medical Genetics
dc.rights	info:eu-repo/semantics/restrictedAccess
dc.rights.uri	https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.subject	Partial trisomy	en_US
dc.title	A new case of proximal 10q partial trisomy	en_US
dc.type	info:eu-repo/semantics/article
dc.identifier.doi	https://doi.org/10.1136/jmg.28.3.205
dc.subject.ocde	https://purl.org/pe-repo/ocde/ford#3.01.02
dc.relation.issn	1468-6244

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