Original Research
Published on 24 Aug 2021
Transmission of a Novel Imprinting Center Deletion Associated With Prader–Willi Syndrome Through Three Generations of a Chinese Family: Case Presentation, Differential Diagnosis, and a Lesson Worth Thinking About
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2021.630650
- 8,101 views
- 2 citations
