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DC Field | Value | Language |
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dc.contributor.author | Santos, Rita de Cassia Stocco dos | pt_BR |
dc.contributor.author | Castro, Nelson Henrique Carvalho de | pt_BR |
dc.contributor.author | Holmes, Lillia | pt_BR |
dc.contributor.author | Beçak, Willy | pt_BR |
dc.contributor.author | Tackels-Horne, Darci | pt_BR |
dc.contributor.author | Lindsey, Charles Julian | pt_BR |
dc.contributor.author | Lubs, Hebert A. | pt_BR |
dc.contributor.author | Stevenson, Robert David | pt_BR |
dc.contributor.author | Schwartz, Charles E. | pt_BR |
dc.date.accessioned | 2019-09-12T16:53:23Z | - |
dc.date.available | 2019-09-12T16:53:23Z | - |
dc.date.issued | 2003 | - |
dc.citation.volume | 118A | pt_BR |
dc.citation.issue | 3 | pt_BR |
dc.citation.spage | 255 | - |
dc.citation.epage | 259 | - |
dc.identifier.doi | 10.1002/ajmg.a.20021 | pt_BR |
dc.identifier.issn | 1552-4825 | - |
dc.identifier.issn | 1552-4833 | - |
dc.identifier.uri | http://repositorio.unitau.br/jspui/handle/20.500.11874/2521 | - |
dc.description.abstract | Mental 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.abstract | O 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.provenance | Made available in DSpace on 2019-09-12T16:53:23Z (GMT). No. of bitstreams: 0 Previous issue date: 2003 | en |
dc.description.sponsorship | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) | pt_BR |
dc.language | Inglês | pt_BR |
dc.publisher | Wiley | - |
dc.publisher.country | Estados Unidos | pt_BR |
dc.relation.ispartof | American Journal of Medical Genetics Part A | - |
dc.rights | Acesso Restrito | pt_BR |
dc.source | Web of Science | pt_BR |
dc.subject.other | Xlmr | en |
dc.subject.other | Xp11.3-Q21.3 | en |
dc.subject.other | Stocco Dos Santos | en |
dc.subject.other | Linkage | en |
dc.subject.other | Hereditary Bullous Dystrophy | en |
dc.subject.other | Chromosome Inactivation | en |
dc.subject.other | Macular Type | en |
dc.subject.other | Gene | en |
dc.subject.other | Maps | en |
dc.title | Stocco dos Santos X-linked mental retardation syndrome: Clinical elucidation and localization to Xp11.3-Xq21.3 | en |
dc.title.alternative | Síndrome de retardo mental ligado ao X de Stocco dos Santos: elucidação clínica e localização para Xp11.3 – Xq21.3 | pt_BR |
dc.type | Artigo de Periódico | pt_BR |
dc.contributor.orcid | Stocco, Rita de Cassia https://orcid.org/0000-0002-2375-5567 | pt_BR |
dc.contributor.researcherid | Stocco, Rita de Cassia/F-2445-2012 | pt_BR |
dc.identifier.wos | WOS:000182401500009 | - |
dc.description.affiliation | Inst 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.wosarea | Genetics & Heredity | en |
dc.subject.researcharea | Genetics & Heredity | en |
Appears in Collections: | Artigos de Periódicos |
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