Cite
HARVARD Citation
Schanze, D. et al. (n.d.). Deletions in the 3′ Part of the NFIX Gene Including a Recurrent Alu‐Mediated Deletion of Exon 6 and 7 Account for Previously Unexplained Cases of Marshall–Smith Syndrome. Human mutation. 35 (9), pp. 1092-1100. [Online].