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For: Jackson CC, Best L, Lorenzo L, Casanova JL, Wacker J, Bertz S, Agaimy A, Harrer T. A Multiplex Kindred with Hennekam Syndrome due to Homozygosity for a CCBE1 Mutation that does not Prevent Protein Expression. J Clin Immunol 2016;36:19-27. [PMID: 26686525 DOI: 10.1007/s10875-015-0225-6] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 1.1] [Reference Citation Analysis]
Number Citing Articles
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3 Souza MR, Ibelli AMG, Savoldi IR, Cantão ME, Peixoto JO, Mores MAZ, Lopes JS, Coutinho LL, Ledur MC. Transcriptome analysis identifies genes involved with the development of umbilical hernias in pigs. PLoS One 2020;15:e0232542. [PMID: 32379844 DOI: 10.1371/journal.pone.0232542] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
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5 Ozen A. CHAPLE syndrome uncovers the primary role of complement in a familial form of Waldmann's disease. Immunol Rev 2019;287:20-32. [PMID: 30565236 DOI: 10.1111/imr.12715] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 3.3] [Reference Citation Analysis]
6 Zhao YR, Liu H, Xiao LM, Jin CG, Zhang ZP, Yang CG. The clinical significance of CCBE1 expression in human colorectal cancer. Cancer Manag Res 2018;10:6581-90. [PMID: 30555263 DOI: 10.2147/CMAR.S181770] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 1.2] [Reference Citation Analysis]
7 Melber DJ, Andreasen TS, Mao R, Tvrdik T, Miller CE, Moore TR, Woelkers DA, Lamale-Smith LM. Novel mutation in CCBE 1 as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia-lymphedema syndrome-1. Clin Case Rep 2018;6:2358-63. [PMID: 30564329 DOI: 10.1002/ccr3.1804] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
8 Crawford J, Bower NI, Hogan BM, Taft RJ, Gabbett MT, Mcgaughran J, Simons C. Expanding the genotypic spectrum of CCBE1 mutations in Hennekam syndrome. Am J Med Genet 2016;170:2694-7. [DOI: 10.1002/ajmg.a.37803] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.9] [Reference Citation Analysis]
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