For: | Yuan N, Lu L, Xing XP, Wang O, Jiang Y, Wu J, He MH, Wang XJ, Cao LW. Clinical and genetic features of Kenny-Caffey syndrome type 2 with multiple electrolyte disturbances: A case report. World J Clin Cases 2023; 11(10): 2290-2300 [PMID: 37122511 DOI: 10.12998/wjcc.v11.i10.2290] |
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URL: | https://www.wjgnet.com/2307-8960/full/v11/i10/2290.htm |
Number | Citing Articles |
1 |
Xuefei Chen, Chaochun Zou. Further delineation of phenotype and genotype of Kenny–Caffey syndrome type 2 (phenotype and genotype of KCS type 2). Molecular Genetics & Genomic Medicine 2024; 12(4) doi: 10.1002/mgg3.2433
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2 |
Kyriaki Hatziagapiou, Amalia Sertedaki, Vasiliki Dermentzoglou, Nataša Čurović Popović, George I. Lambrou, Louis Papageorgiou, Trias Thireou, Christina Kanaka-Gantenbein, Sophia D. Sakka. Kenny–Caffey Syndrome Type 2 (KCS2): A New Case Report and Patient Follow-Up Optimization. Journal of Clinical Medicine 2024; 14(1): 118 doi: 10.3390/jcm14010118
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