Search

Author/Creator Ji, Yiting

1. A novel 1p33p32.2 deletion involving SCP2, ORC1, and DAB1 genes in a patient with craniofacial dysplasia, short stature, developmental delay, and leukoencephalopathy: A case report. Issue 45 (6th November 2020)

Authors:
Jiang, Maoying; Wang, Shanlin; Li, Fei; Geng, Juan; Ji, Yiting; Li, Ke; Jiang, Xiaodong
Other Names:
Saranathan. Maya section editor.
Journal:
Medicine
Issue:
Volume 99:Issue 45(2020)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Altered social cognition and connectivity of default mode networks in the co-occurrence of autistic spectrum disorder and attention deficit hyperactivity disorder. (August 2019)

Authors:
Wang, Kai; Xu, Mingyu; Ji, Yiting; Zhang, Lingli; Du, Xiujuan; Li, Jijun; Luo, Qiang; Li, Fei
Journal:
Australian and New Zealand journal of psychiatry
Issue:
Volume 53:Number 8(2019)
Page Start:
760
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗