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Cited by in F6Publishing
For: Deeb A, Afandi O, Attia S, Fatih AE. 3-M syndrome: a novel CUL7 mutation associated with respiratory distress and a good response to GH therapy. Endocrinol Diabetes Metab Case Rep. 2015;2015:150012. [PMID: 25945256 DOI: 10.1530/EDM-15-0012] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.4] [Reference Citation Analysis]
Number Citing Articles
1 Keskin M, Muratoğlu Şahin N, Kurnaz E, Bayramoğlu E, Savaş Erdeve Ş, Aycan Z, Çetinkaya S. A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene. J Clin Res Pediatr Endocrinol 2017;9:91-4. [PMID: 27796265 DOI: 10.4274/jcrpe.3238] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 1.3] [Reference Citation Analysis]
2 Takizaki N, Tsurusaki Y, Katsumata K, Enomoto Y, Murakami H, Muroya K, Ishikawa H, Aida N, Nishimura G, Kurosawa K. Novel CUL7 biallelic mutations alter the skeletal phenotype of 3M syndrome. Hum Genome Var 2020;7:1. [PMID: 32047638 DOI: 10.1038/s41439-020-0090-6] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Hu L, Wang X, Jin T, Han Y, Liu J, Jiang M, Yan S, Fu X, An B, Huang S. Identification of two CUL7 variants in two Chinese families with 3-M syndrome by whole-exome sequencing. J Clin Lab Anal 2020;34:e23265. [PMID: 32141654 DOI: 10.1002/jcla.23265] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
4 Takatani T, Shiohama T, Takatani R, Shimojo N. A novel CUL7 mutation in a Japanese patient with 3M syndrome. Hum Genome Var 2018;5:30. [PMID: 30374406 DOI: 10.1038/s41439-018-0029-3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
5 Yang LL, Liang SS. Study on pathogenic genes of dwarfism disease by next-generation sequencing. World J Clin Cases 2021; 9(7): 1600-1609 [PMID: 33728303 DOI: 10.12998/wjcc.v9.i7.1600] [Reference Citation Analysis]