Cite
MLA Citation
Wayne W K Lam et al.. “Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation.” Journal of medical genetics, vol. 36, no. 7, 1999, pp. 518–523. http://access.bl.uk/ark:/81055/vdc_100137789279.0x000040