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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/63774
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dc.contributor.authorRichieri-Costa, A.-
dc.contributor.authorOpitz, J. M.-
dc.date.accessioned2014-05-27T01:54:29Z-
dc.date.accessioned2016-10-25T18:12:06Z-
dc.date.available2014-05-27T01:54:29Z-
dc.date.available2016-10-25T18:12:06Z-
dc.date.issued1986-12-01-
dc.identifierhttp://dx.doi.org/10.1002/ajmg.1320250624-
dc.identifier.citationAmerican journal of medical genetics. Supplement, v. 2, p. 195-206.-
dc.identifier.issn1040-3787-
dc.identifier.urihttp://hdl.handle.net/11449/63774-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/63774-
dc.description.abstractWe report on five Brazilian patients from three unrelated families with congenital anomalies of the upper limbs. Ulnar aplasia/hypoplasia was the main reason for examining these patients. Evidence for existence of an ulnar developmental field is based on genetic heterogeneity. Clinical and genetic aspects of the ulnar ray defects are discussed.en
dc.format.extent195-206-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectcongenital malformation-
dc.subjectembryology-
dc.subjectinfant-
dc.subjectpreschool child-
dc.subjectradiography-
dc.subjectrecessive gene-
dc.subjectsyndrome-
dc.subjectulna-
dc.subjectSupport, Non-U.S. Gov't-
dc.subjectSyndrome-
dc.titleUlnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families.en
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.identifier.doi10.1002/ajmg.1320250624-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofAmerican journal of medical genetics. Supplement-
dc.identifier.scopus2-s2.0-0022932236-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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