Author

E. Bonifaci

OpenAlex ID: A5033988331

Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment

1983 · M. Fraccaro, O. Zuffardi, et al. · Human Genetics · 49

Works count: 1

Citation count: 49

H-index: 1

I10-index: 1