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dc.contributor.authorTajara, E. H.
dc.contributor.authorVarella-Garcia, M.
dc.contributor.authorTonelli Gusson, A. C.
dc.date.accessioned2014-05-27T05:20:55Z
dc.date.available2014-05-27T05:20:55Z
dc.date.issued1989-01-01
dc.identifierhttp://dx.doi.org/10.1002/ajmg.1320320212
dc.identifier.citationAmerican Journal of Medical Genetics, v. 32, n. 2, p. 192-194, 1989.
dc.identifier.issn0148-7299
dc.identifier.urihttp://hdl.handle.net/11449/63884
dc.description.abstractAn interstitial deletion of 7q21 was found in a boy with mental retardation, microcephaly, convergent strabismus, micrognathia, genital anomalies, and other findings, including ectrodactyly.en
dc.format.extent192-194
dc.language.isoeng
dc.relation.ispartofAmerican Journal of Medical Genetics
dc.sourceScopus
dc.subjectchromosome 7q
dc.subjectchromosome deletion 7
dc.subjectcytology
dc.subjectectrodactyly
dc.subjectheredity
dc.subjectinfant
dc.subjectmental retardation malformation syndrome
dc.subjectmicrocephaly
dc.subjectmicrognathia
dc.subjectpartial monosomy 7
dc.subjectpriority journal
dc.subjectAbnormalities, Multiple
dc.subjectCase Report
dc.subjectChromosome Deletion
dc.subjectChromosomes, Human, Pair 7
dc.subjectClubfoot
dc.subjectFingers
dc.subjectMental Retardation
dc.subjectSupport, Non-U.S. Gov't
dc.subjectSyndrome
dc.subjectToes
dc.titleInterstitial long-arm deletion of chromosome 7 and ectrodactylyen
dc.typeArtigo
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.identifier.doi10.1002/ajmg.1320320212
dc.rights.accessRightsAcesso restrito
dc.identifier.scopus2-s2.0-0024517762
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