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

N. Hoppman-Chaney, K. Wain, P. R. Seger, D. W. Superneau, J. C. Hodge

Research output: Contribution to journal › Article › peer-review

69 Scopus citations

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Medicine & Life Sciences