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Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families.

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dc.contributor.authorRichieri-Costa, A.
dc.contributor.authorOpitz, J. M.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T01:54:29Z
dc.date.available2014-05-27T01:54:29Z
dc.date.issued1986-12-01
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.identifierhttp://dx.doi.org/10.1002/ajmg.1320250624
dc.identifier.citationAmerican journal of medical genetics. Supplement, v. 2, p. 195-206.
dc.identifier.doi10.1002/ajmg.1320250624
dc.identifier.issn1040-3787
dc.identifier.scopus2-s2.0-0022932236
dc.identifier.urihttp://hdl.handle.net/11449/63774
dc.language.isoeng
dc.relation.ispartofAmerican journal of medical genetics. Supplement
dc.rights.accessRightsAcesso restrito
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.typeArtigo
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dspace.entity.typePublication

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