A Chinese child with hyperpigmentation diagnosed with familial glucocorticoid deficiency type 1 using whole-exome sequencing

Saved in:

Bibliographic Details
Main Authors:	Junke Xia (Author), Zhihui Jiao (Author), Zhenhua Zhao (Author), Jing Wu (Author), Xiangdong Kong (Author)
Format:	Book
Published:	Elsevier, 2021-03-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
Tags:	Add Tag No Tags, Be the first to tag this record!

Internet

Holdings details from 3rd Floor Main Library
Call Number:	A1234.567
Copy 1	Available