Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects

Detalhes bibliográficos
Autor(a) principal: Lucon,Danielle R.
Data de Publicação: 2006
Outros Autores: Zanchetta,Luciene M., Cavalcanti,Denise P.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Genetics and Molecular Biology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572006000100006
Resumo: Chimerism is rare in humans and is usually discovered accidentally when a 46,XX and 46,XY karyotype is found in a same individual. We describe a malformed female infant with neural tube defect (NTD) and a 47,XY,+21[5]/46,XX[30] karyotype.
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spelling Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defectschimerismanencephalytrisomy 21Chimerism is rare in humans and is usually discovered accidentally when a 46,XX and 46,XY karyotype is found in a same individual. We describe a malformed female infant with neural tube defect (NTD) and a 47,XY,+21[5]/46,XX[30] karyotype.Sociedade Brasileira de Genética2006-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572006000100006Genetics and Molecular Biology v.29 n.1 2006reponame:Genetics and Molecular Biologyinstname:Sociedade Brasileira de Genética (SBG)instacron:SBG10.1590/S1415-47572006000100006info:eu-repo/semantics/openAccessLucon,Danielle R.Zanchetta,Luciene M.Cavalcanti,Denise P.eng2006-03-10T00:00:00Zoai:scielo:S1415-47572006000100006Revistahttp://www.gmb.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||editor@gmb.org.br1678-46851415-4757opendoar:2006-03-10T00:00Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG)false
dc.title.none.fl_str_mv Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects
title Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects
spellingShingle Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects
Lucon,Danielle R.
chimerism
anencephaly
trisomy 21
title_short Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects
title_full Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects
title_fullStr Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects
title_full_unstemmed Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects
title_sort Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects
author Lucon,Danielle R.
author_facet Lucon,Danielle R.
Zanchetta,Luciene M.
Cavalcanti,Denise P.
author_role author
author2 Zanchetta,Luciene M.
Cavalcanti,Denise P.
author2_role author
author
dc.contributor.author.fl_str_mv Lucon,Danielle R.
Zanchetta,Luciene M.
Cavalcanti,Denise P.
dc.subject.por.fl_str_mv chimerism
anencephaly
trisomy 21
topic chimerism
anencephaly
trisomy 21
description Chimerism is rare in humans and is usually discovered accidentally when a 46,XX and 46,XY karyotype is found in a same individual. We describe a malformed female infant with neural tube defect (NTD) and a 47,XY,+21[5]/46,XX[30] karyotype.
publishDate 2006
dc.date.none.fl_str_mv 2006-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572006000100006
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572006000100006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1415-47572006000100006
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Genética
publisher.none.fl_str_mv Sociedade Brasileira de Genética
dc.source.none.fl_str_mv Genetics and Molecular Biology v.29 n.1 2006
reponame:Genetics and Molecular Biology
instname:Sociedade Brasileira de Genética (SBG)
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collection Genetics and Molecular Biology
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