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Cited by in CrossRef
For: Wu JL, Li XL, Chen SM, Lan XP, Chen JJ, Li XY, Wang W. A three-year clinical investigation of a Chinese child with craniometaphyseal dysplasia caused by a mutated ANKH gene. World J Clin Cases 2021; 9(8): 1853-1862 [PMID: 33748234 DOI: 10.12998/wjcc.v9.i8.1853]
URL: https://www.wjgnet.com/2307-8960/full/v9/i8/1853.htm
Number Citing Articles
1
Julio Soto Barros, Demetrios Braddock, Thomas O. Carpenter. Hypophosphatemic rickets: An unexplained early feature of craniometaphyseal dysplasiaBone Reports 2023; 19: 101707 doi: 10.1016/j.bonr.2023.101707