Cite
MLA Citation
Denny Schanze et al.. “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, vol. 35, no. 9, n.d., pp. 1092–1100. http://access.bl.uk/ark:/81055/vdc_100024895408.0x00002e