Skip to content
Log in
Sponsored AI AM CLAUDE, A Beginner's Guide: Learn the basics of working with AI AI AM CLAUDE, A Beginner's Guide: Learn the basics of working with AI

Author

Qiong Zhou

View on Semantic Scholar

1 paper indexed here

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Review Open access Oct 2026

Case Report: Concurrent maternal uniparental disomy-type Prader-Willi syndrome and X-linked G6PD deficiency—an area of focus on multi-gene screening for imprinting disorders

Prader-Willi syndrome (PWS) is a rare imprinting disorder caused by functional impairment of imprinted genes within the paternal 15q11.2-q13 region. Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked hereditary disorder. Cases describing the coexistence of maternal uniparental disomy (UPD)-type PWS...

Qiong Zhou, Jia-Ming Yuan, Chao-Chun Zou · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.