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

dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T01:54:29Z
dc.date.accessioned2022-10-05T17:23:43Z
dc.date.available2014-05-27T01:54:29Z
dc.date.available2022-10-05T17:23:43Z
dc.date.created2014-05-27T01:54:29Z
dc.date.issued1986-12-01
dc.identifierAmerican journal of medical genetics. Supplement, v. 2, p. 195-206.
dc.identifier1040-3787
dc.identifierhttp://hdl.handle.net/11449/63774
dc.identifier10.1002/ajmg.1320250624
dc.identifier2-s2.0-0022932236
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3913953
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.
dc.languageeng
dc.relationAmerican journal of medical genetics. Supplement
dc.rightsAcesso 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.
dc.typeArtigo


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