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dc.contributor.authorSantos, Rita de Cassia Stocco dospt_BR
dc.contributor.authorCastro, Nelson Henrique Carvalho dept_BR
dc.contributor.authorHolmes, Lilliapt_BR
dc.contributor.authorBeçak, Willypt_BR
dc.contributor.authorTackels-Horne, Darcipt_BR
dc.contributor.authorLindsey, Charles Julianpt_BR
dc.contributor.authorLubs, Hebert A.pt_BR
dc.contributor.authorStevenson, Robert Davidpt_BR
dc.contributor.authorSchwartz, Charles E.pt_BR
dc.date.accessioned2019-09-12T16:53:23Z-
dc.date.available2019-09-12T16:53:23Z-
dc.date.issued2003-
dc.citation.volume118Apt_BR
dc.citation.issue3pt_BR
dc.citation.spage255-
dc.citation.epage259-
dc.identifier.doi10.1002/ajmg.a.20021pt_BR
dc.identifier.issn1552-4825-
dc.identifier.issn1552-4833-
dc.identifier.urihttp://repositorio.unitau.br/jspui/handle/20.500.11874/2521-
dc.description.abstractMental retardation (MR) affects an estimated 2-3% of the population. A considerable fraction of mental retardation is due to X-linked genes. Of these genes, about 136 are responsible for syndromic X-linked MR (XLMR). One such XLMR syndrome, Stocco dos Santos, was first described in 1991. This family was re-visited, which allowed further delineation of the clinical phenotype. Additionally, linkage analysis was conducted, which resulted in the localization of this XLMR syndrome to the pericentric region, Xp11.3 to Xq21.1, with a maximum LOD score of 3.14 at loci AR and DXS983. (C) 2003 Wiley-Liss, Inc.en
dc.description.abstractO retardo mental (RM) afeta cerca de 2 a 3% da população. Uma fração considerável de retardo mental é devida a genes ligados ao X. Desses genes, cerca de 136 são responsáveis ​​pela RM sindrômica ligada ao X (XLMR). Uma dessas síndromes XLMR, Stocco dos Santos, foi descrita pela primeira vez em 1991. Essa família foi visitada novamente, o que permitiu delinear ainda mais o fenótipo clínico. Além disso, foi realizada análise de ligação, que resultou na localização dessa síndrome XLMR na região pericêntrica, Xp11.3 a Xq21.1, com uma pontuação máxima de LOD de 3,14 nos loci AR e DXS983. © 2003 Wiley-Liss, Inc.pt_BR
dc.description.provenanceMade available in DSpace on 2019-09-12T16:53:23Z (GMT). No. of bitstreams: 0 Previous issue date: 2003en
dc.description.sponsorshipEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)pt_BR
dc.languageInglêspt_BR
dc.publisherWiley-
dc.publisher.countryEstados Unidospt_BR
dc.relation.ispartofAmerican Journal of Medical Genetics Part A-
dc.rightsAcesso Restritopt_BR
dc.sourceWeb of Sciencept_BR
dc.subject.otherXlmren
dc.subject.otherXp11.3-Q21.3en
dc.subject.otherStocco Dos Santosen
dc.subject.otherLinkageen
dc.subject.otherHereditary Bullous Dystrophyen
dc.subject.otherChromosome Inactivationen
dc.subject.otherMacular Typeen
dc.subject.otherGeneen
dc.subject.otherMapsen
dc.titleStocco dos Santos X-linked mental retardation syndrome: Clinical elucidation and localization to Xp11.3-Xq21.3en
dc.title.alternativeSíndrome de retardo mental ligado ao X de Stocco dos Santos: elucidação clínica e localização para Xp11.3 – Xq21.3pt_BR
dc.typeArtigo de Periódicopt_BR
dc.contributor.orcidStocco, Rita de Cassia https://orcid.org/0000-0002-2375-5567pt_BR
dc.contributor.researcheridStocco, Rita de Cassia/F-2445-2012pt_BR
dc.identifier.wosWOS:000182401500009-
dc.description.affiliationInst Butantan, Genet Lab, Sao Paulo, Brazil; Univ Fed Sao Paulo, Dept Biofis, Sao Paulo, SP, Brazil; Univ Miami, Sch Med, Dept Pediat, Miami, FL USA; Universidade de Taubaté (Unitau), Dept Biol Mol; Greenwood Genet Ctr, JC Self Res Inst, Ctr Mol Studies, Greenwood, SC 29646 USA-
dc.subject.wosareaGenetics & Heredityen
dc.subject.researchareaGenetics & Heredityen
Appears in Collections:Artigos de Periódicos

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