BPG is committed to discovery and dissemination of knowledge
Cited by in CrossRef
For: Li J, Chen LN, He HL. CDKN1C gene mutation causing familial Silver–Russell syndrome: A case report and review of literature. World J Clin Cases 2023; 11(19): 4655-4663 [PMID: 37469742 DOI: 10.12998/wjcc.v11.i19.4655]
URL: https://www.wjgnet.com/2307-8960/full/v11/i19/4655.htm
Number Citing Articles
1
Uttara Kurup, David B N Lim, Helena Palau, Avinaash V Maharaj, Miho Ishida, Justin H Davies, Helen L Storr. Approach to the Patient With Suspected Silver-Russell SyndromeThe Journal of Clinical Endocrinology & Metabolism 2024;  doi: 10.1210/clinem/dgae423