• Users Online: 531
  • Home
  • Print this page
  • Email this page
Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Contacts Login

  Reader Comments

Year : 2019 | Volume:  32 | Issue Number:  3

SHORT REPORT

Novel mutation in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene associated with intrafamilial heterogeneity in three boys with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism from India

Mohan Sony, Danda Sumita, Mathai Sarah, Simon Anna

Add Your Comments
 
No one has added comments on this article. Click here to add your remarks


 

Back To Article
Submit articles
Most popular articles
Joiu us as a reviewer
Email alerts
Ted Talks / Other Talks