Trisomy 9: An additional case with unique manifestations

dc.contributor.author	de Michelena, María
dc.contributor.author	Sánchez, Raul
dc.contributor.author	Muñoz, Pedro
dc.contributor.author	Cabello,Emilio
dc.contributor.author	Rojas,Pablo
dc.contributor.author	de Olazaval, Eduardo
dc.date.accessioned	2022-10-10T03:26:12Z
dc.date.available	2022-10-10T03:26:12Z
dc.date.issued	1992
dc.identifier.uri	https://hdl.handle.net/20.500.12866/12345
dc.description.abstract	We report on an infant with multiple congenital anomalies and mosaic trisomy 9. Clinical findings are presented, and compared with those of the 24 cases previously reported. Some unusual characteristics found in this patient include macrocephaly, an extreme degree of palatal hypoplasia, and abnormally shaped long bones.	en_US
dc.language.iso	eng
dc.publisher	Wiley
dc.relation.ispartofseries	American 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	Trisomy 9	en_US
dc.title	Trisomy 9: An additional case with unique manifestations	en_US
dc.type	info:eu-repo/semantics/article
dc.identifier.doi	https://doi.org/10.1002/ajmg.1320430409
dc.subject.ocde	https://purl.org/pe-repo/ocde/ford#3.01.02
dc.relation.issn	0148-7299

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