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Mar 16, 2021 (publication date) through May 5, 2026
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World Journal of Clinical Cases
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2307-8960
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| 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] |
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| 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] |
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| 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 dysplasia. Bone Reports 2023; 19: 101707 doi: 10.1016/j.bonr.2023.101707
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| 2 |
Jaynee Chauhan, Rachael Scullion, Siva Sithambaram. Craniosynostosis in craniometaphyseal dysplasia: an expansion of phenotype. Clinical Dysmorphology 2026; doi: 10.1097/MCD.0000000000000564
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