Please use this identifier to cite or link to this item: http://repositorio.unitau.br/jspui/handle/20.500.11874/2520
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dc.contributor.authorCastro, NHCpt_BR
dc.contributor.authordos Santos, RCSpt_BR
dc.contributor.authorNelson, Rpt_BR
dc.contributor.authorBecak, Wpt_BR
dc.contributor.authorHane, Bpt_BR
dc.contributor.authorLindsey, CJpt_BR
dc.contributor.authorLubs, HApt_BR
dc.contributor.authorStevenson, REpt_BR
dc.contributor.authorSchwartz, CEpt_BR
dc.date.accessioned2019-09-12T16:53:23Z-
dc.date.available2019-09-12T16:53:23Z-
dc.date.issued2003-
dc.citation.volume118Apt_BR
dc.citation.issue1pt_BR
dc.citation.spage49-
dc.citation.epage51-
dc.identifier.doi10.1002/ajmg.a.10888pt_BR
dc.identifier.issn0148-7299-
dc.identifier.urihttp://repositorio.unitau.br/jspui/handle/20.500.11874/2520-
dc.description.abstractThis 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.abstractEste 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.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-Liss-
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.otherShashi Xlmren
dc.subject.otherHaplotype Analysisen
dc.subject.otherXq26-Q27en
dc.subject.otherMapsen
dc.titleShashi XLMR syndrome: Report of a second familyen
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:000182401200008-
dc.description.affiliationGreenwood 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.wosareaGenetics & Heredityen
dc.subject.researchareaGenetics & Heredityen
Appears in Collections:Artigos de Periódicos

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