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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; 109(10): e1889 doi: 10.1210/clinem/dgae423
2
Ekaterina Kim, Anastasiia Lavreniuk, Olga Spasskaya, Anna Eremkina, Rustam Salimkhanov, Liliya Urusova, Natalia Tarbaeva, Sergey Popov, Victoria Zakharova, Natalia Mokrysheva. Case report: Relapse of intrathyroidal parathyroid carcinoma in a patient with novel variants in MET and CDKN1C genesFrontiers in Oncology 2025; 14 doi: 10.3389/fonc.2024.1441083