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DC Field | Value | Language |
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dc.contributor.author | Castro, NHC | pt_BR |
dc.contributor.author | dos Santos, RCS | pt_BR |
dc.contributor.author | Nelson, R | pt_BR |
dc.contributor.author | Becak, W | pt_BR |
dc.contributor.author | Hane, B | pt_BR |
dc.contributor.author | Lindsey, CJ | pt_BR |
dc.contributor.author | Lubs, HA | pt_BR |
dc.contributor.author | Stevenson, RE | pt_BR |
dc.contributor.author | Schwartz, CE | 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 | 1 | pt_BR |
dc.citation.spage | 49 | - |
dc.citation.epage | 51 | - |
dc.identifier.doi | 10.1002/ajmg.a.10888 | pt_BR |
dc.identifier.issn | 0148-7299 | - |
dc.identifier.uri | http://repositorio.unitau.br/jspui/handle/20.500.11874/2520 | - |
dc.description.abstract | This report describes a family with mental retardation in two brothers. The pedigree is consistent with either X-linked mental retardation or autosomal recessive inheritance. The clinical features consist of coarse face, prominent lower lip, large testes, and obesity. This same constellation of findings was observed in a family with X-linked mental retardation (XLMR) reported by Shashi et al. [2000: Am J Hum Genet 66:469-479]. Furthermore, haplotype analysis was consistent with localization of the Shashi XLMR syndrome in Xq26-q27. Thus, the family likely represents a second occurrence of the Shashi XLMR syndrome. (C) 2003 Wiley-Liss, Inc. | en |
dc.description.abstract | Este relatório descreve uma família com retardo mental em dois irmãos. O pedigree é consistente com retardo mental ligado ao X ou herança autossômica recessiva. As características clínicas consistem em face grossa, lábio inferior proeminente, testículos grandes e obesidade. Essa mesma constelação de achados foi observada em uma família com retardo mental ligado ao X (XLMR) relatado por Shashi et al. [2000: Am J Hum Genet 66: 469–479]. Além disso, a análise do haplótipo foi consistente com a localização da síndrome de Shashi XLMR em Xq26 ‐ q27. Assim, a família provavelmente representa uma segunda ocorrência da síndrome de Shashi XLMR. © 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-Liss | - |
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 | Shashi Xlmr | en |
dc.subject.other | Haplotype Analysis | en |
dc.subject.other | Xq26-Q27 | en |
dc.subject.other | Maps | en |
dc.title | Shashi XLMR syndrome: Report of a second family | en |
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:000182401200008 | - |
dc.description.affiliation | Greenwood Genet Ctr, JC Self Res Inst, Ctr Mol Studies, Greenwood, SC 29646 USA; Inst Butantan, Genet Lab, Sao Paulo, Brazil; Univ Fed Sao Paulo, Dept Biofis, Sao Paulo, Brazil; Univ Miami, Sch Med, Dept Pediat, Miami, FL 33152 USA; Universidade de Taubaté (Unitau), Sao Paulo, Brazil | - |
dc.subject.wosarea | Genetics & Heredity | en |
dc.subject.researcharea | Genetics & Heredity | en |
Appears in Collections: | Artigos de Periódicos |
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