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Cited by in CrossRef
For: Fontana P, Passaretti FF, Maioli M, Cantalupo G, Scarano F, Lonardo F. Clinical and molecular spectrum of Wiedemann-Steiner syndrome, an emerging member of the chromatinopathy family. World J Med Genet 2020; 9(1): 1-11 [DOI: 10.5496/wjmg.v9.i1.1]
URL: https://www.wjgnet.com/2220-3184/full/v9/i1/1.htm
Number Citing Articles
1
岭 马. A Case of Wiedemann-Steiner Syndrome with Short Stature Caused by a Novel Mutation in KMT2A GeneAdvances in Clinical Medicine 2021; 11(07): 2914 doi: 10.12677/ACM.2021.117422