Universidad Peruana Cayetano Heredia

Trisomy 9: An additional case with unique manifestations

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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.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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