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Cited by in F6Publishing
For: Piccolo G, d'Annunzio G, Amadori E, Riva A, Borgia P, Tortora D, Maghnie M, Minetti C, Gitto E, Iacomino M, Baldassari S, Fiorillo C, Zara F, Striano P, Salpietro V. Neuromuscular and Neuroendocrinological Features Associated With ZC4H2-Related Arthrogryposis Multiplex Congenita in a Sicilian Family: A Case Report. Front Neurol 2021;12:704747. [PMID: 34322088 DOI: 10.3389/fneur.2021.704747] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Muhammad H, Haryana SM, Magetsari R, Karsten S, Saraswati PA. Genes on syndromic and idiopathic CTEV: A systematic review. International Journal of Surgery Open 2022;47:100547. [DOI: 10.1016/j.ijso.2022.100547] [Reference Citation Analysis]
2 Sun J, Cai Q, Xu M, Liu Y, Li W, Li J, Ma L, Cai C, Gong X, Zeng Y, Ren Z, Zeng F. Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome due to a Novel Nonsense Mutation in the ZC4H2 Gene. Genes 2022;13:1558. [DOI: 10.3390/genes13091558] [Reference Citation Analysis]
3 Ahn JY, Kim SY, Lim BC, Kim KJ, Chae J. Variable Phenotypes of ZC4H2-Associated Rare Disease in Six Patients. Ann Child Neurol 2022;30:120-126. [DOI: 10.26815/acn.2022.00129] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Comlekoglu T, Kumar V, King K, Al Saif H, Li R, Couser N. Ophthalmic abnormalities in Wieacker-Wolff syndrome. J AAPOS 2022;26:91-3. [PMID: 35121145 DOI: 10.1016/j.jaapos.2021.10.010] [Reference Citation Analysis]