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For: Imagawa E, Konuma T, Cork EE, Diaz GA, Oishi K. A novel missense variant in RBM10 can cause a mild form of TARP syndrome with developmental delay and dysmorphic features. Clin Genet 2020;98:606-12. [PMID: 32812661 DOI: 10.1111/cge.13835] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
Number Citing Articles
1 Daicheng H, Shiwen X, Jingxuan Z, Junbo H, Bo W. A Frameshift RBM10 Variant Associated With TARP Syndrome. Front Genet 2022;13:922048. [DOI: 10.3389/fgene.2022.922048] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Augustine D, Sowmya S, Haragannavar VC, Gujjar N, Patil S. Genetics of Pierre Robin Syndrome/Sequence. eLS 2022. [DOI: 10.1002/9780470015902.a0029427] [Reference Citation Analysis]
3 Poulton C, Baynam G, Pugh K, Mason M, Kiraly-Borri C, Gration D, Dreyer L, Viti L, Agostino M, Heng JI. Further evidence for distinct traits associated with RBM10 missense variants. Clin Genet 2022. [PMID: 35645043 DOI: 10.1111/cge.14163] [Reference Citation Analysis]
4 Manotas H, Payán-Gómez C, Roa MF, Piñeros JG. TARP syndrome associated with renal malformation and optic nerve atrophy. BMJ Case Rep 2021;14:e240601. [PMID: 34031074 DOI: 10.1136/bcr-2020-240601] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Kumps C, D'haenens E, Vergult S, Leus J, van Coster R, Jansen A, Devriendt K, Oostra A, Vanakker OM. Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features. Clin Genet 2021;99:449-56. [PMID: 33340101 DOI: 10.1111/cge.13901] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]