dc.contributorUniv Iowa
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T13:50:11Z
dc.date.available2014-05-20T13:50:11Z
dc.date.created2014-05-20T13:50:11Z
dc.date.issued2003-09-15
dc.identifierAmerican Journal of Medical Genetics Part A. New York: Wiley-liss, v. 122A, n. 1, p. 56-58, 2003.
dc.identifier0148-7299
dc.identifierhttp://hdl.handle.net/11449/17915
dc.identifier10.1002/ajmg.a.20270
dc.identifierWOS:000185097900010
dc.description.abstractThe Richieri-Costa-Pereira syndrome is a rare autosomal recessive disorder characterized by short stature, Robin sequence, cleft mandible, pre/postaxial anomalies and clubfoot. of 15 families reported with this disorder 14 are from Brazil suggesting a founder effect. We studied 15 families using identity-by-descent as a hypothesis to attempt gene localization We have examined through linkage analysis 497 polymorphicmarkers and also performed direct sequencing of exons for 10 candidate genes selected on the basis of their expression in the developing mandible and limb. No evidence for allele sharing at any locus tested or mutations in candidate genes was found. Additional higher resolution mapping, new families and other candidate genes might improve future chances of gene identification. (C) 2003 Wiley-Liss, Inc.
dc.languageeng
dc.publisherWiley-Blackwell
dc.relationAmerican Journal of Medical Genetics Part A
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectRichieri-Costa-Pereira syndrome
dc.subjectcleft mandible
dc.subjectMarshfield markers
dc.titleIdentity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome
dc.typeArtículos de revistas


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