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王红艳
Name (Pinyin):wanghongyan
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Academic Achievements
High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability
Apr 2, 2021
|
Journal:
PLoS One
Document Code:
SY146532
Volume:
7
Issue:
4
Translation or Not:
no
Date of Publication:
Jan 1, 2012
Pre One: Identification of Novel Rare Mutations of DACT1 in Human Neural Tube Defects
Next One: Structural and functional insights into the heme-binding domain of the human soluble guanylate cyclase alpha 2 subunit and heterodimeric alpha 2 beta 1