1.
J Pediatr
; 155(3): 439-43, 2009 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19732585
RESUMO
A phenotypic female with complete androgen insensitivity from a maternally inherited mutation in the androgen receptor had a 47,XXY karyotype. Partial maternal X isodisomy explained the expression of androgen insensitivity despite the presence of 2 X chromosomes.