TY  -  
T1  - Genetics of Müllerian aplasia 
SN  -  /  
UR  - URN:ISBN:978-952-10-9333-3; http://hdl.handle.net/10138/41109 
T3  -  
A1  - Sandbacka, Maria 
A2  -  
PB  - Helsingin yliopisto 
Y1  - 2013 
LA  - eng 
AB  - Müllerian aplasia (MA) is a rare congenital disorder of the female reproductive tract. It involves loss of a functional uterus and upper two thirds of the vagina, resulting in infertility and need of treatment to enable normal sex life. Skeletal and renal structural abnormalities, such as scoliosis and renal agenesis are often associated with MA. The patients are otherwise healthy females with normal secondary sex characteristics and karyotype (46,XX). However, psychosocial problems are often en... 
VO  -  
IS  -  
SP  -  
OP  -  
KW  - medicinsk genetik 
N1  -   
PP  -  
ER  -