Artículos de revistas
Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects
Registro en:
Genetics and Molecular Biology. Sociedade Brasileira de Genética, v. 29, n. 1, p. 36-37, 2006.
1415-4757
S1415-47572006000100006
10.1590/S1415-47572006000100006
Autor
Lucon, Danielle R.
Zanchetta, Luciene M.
Cavalcanti, Denise P.
Institución
Resumen
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. 36 37 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)