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

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

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(Reference retrieved automatically from SciELO through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

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

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Author(s):	Danielle R. Lucon ^[1] ; Luciene M. Zanchetta ^[2] ; Denise P. Cavalcanti ^[3] Total Authors: 3
Affiliation:	^[1] Universidade Estadual de Campinas. Faculdade de Ciências Médicas. Departamento de Genética Médica - Brasil ^[2] Universidade Estadual de Campinas. Faculdade de Ciências Médicas. Departamento de Genética Médica - Brasil ^[3] Universidade Estadual de Campinas. Faculdade de Ciências Médicas. Departamento de Genética Médica - Brasil Total Affiliations: 3
Document type:	Journal article
Source:	GENETICS AND MOLECULAR BIOLOGY; v. 29, n. 1, p. 36-37, 2006-00-00.
Abstract
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. (AU)

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