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

Danielle R. Lucon; Denise P. Cavalcanti; Luciene M. Zanchetta

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

机译：患有无脑和其他先天性缺陷的女婴的嵌合体47，XY，+ 21/46，XX

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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.

机译：嵌合体在人类中很少见，通常是在同一个人中发现46，XX和46，XY核型时偶然发现的。我们描述了畸形的女婴，患有神经管缺陷（NTD）和47，XY，+ 21 [5] / 46，XX [30]核型。

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《Genetics and molecular biology: publication of the Sociedade Brasileira de Genetica》 |2006年第1期|共2页
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Danielle R. Lucon; Denise P. Cavalcanti; Luciene M. Zanchetta;
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中图分类遗传学;
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Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects

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