Search Results - Xiaohan Hou
- Showing 1 - 1 results of 1
-
1
Case Report: Two different acromelic dysplasia phenotypes in a Chinese family caused by a missense mutation in FBN1 and a literature review by Fengyan Tian, Xiao Dong, Ruyue Yuan, Xiaohan Hou, Jing Qing, Yani Li
Published 2024Call Number: Loading…Connect to this object online.
Located: Loading…
Book