Author

PR Seger

Institution: Mayo Clinic

Observed institution: Mayo Clinic

OpenAlex ID: A5063250260

Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype

2012 · N Hoppman‐Chaney, K Wain, et al. · Clinical Genetics · 133

Works count: 1

Citation count: 133

H-index: 1

I10-index: 1